RHCG Rh family C glycoprotein

Information
Symbol
RHCG
Type
protein-coding
Description
Rh family C glycoprotein
Entrez Gene ID
51458
Genome
hg19
Position
chr15:90,014,638-90,039,814
Genome
hg38
Position
chr15:89,471,407-89,496,583
MIM
605381 OMIM
HGNC
HGNC:18140 HGNC
Ensembl
ENSG00000140519 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 62
Ranking
ClinVar
0
0
0
68
0
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.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM C15orf6
SYNONYM PDRC2
SYNONYM RHGK
SYNONYM SLC42A3
MIM 605381 OMIM
HGNC HGNC:18140 HGNC
Ensembl ENSG00000140519 Ensembl
AllianceGenome HGNC:18140
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000268122.9 hg38 chr15 89,471,407 89,496,583 25,177
ENST00000268122.9 hg19 chr15 90,014,638 90,039,814 25,177
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