IGHV3-23 immunoglobulin heavy variable 3-23
Information
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
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Variants
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | DP47 |
SYNONYM | IGHV323 |
SYNONYM | V3-23 |
SYNONYM | VH26 |
MIM | 611939 OMIM |
HGNC | HGNC:5588 HGNC |
Ensembl | ENSG00000211949 Ensembl |
IMGT/GENE-DB | IGHV3-23 |
AllianceGenome | HGNC:5588 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000390609.3 | hg38 | chr14 | 106,268,606 | 106,269,140 | 535 |
ENST00000390609.3 | hg19 | chr14 | 106,725,199 | 106,725,733 | 535 |
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