RHBG Rh family B glycoprotein

Information
Symbol
RHBG
Type
protein-coding
Description
Rh family B glycoprotein
Entrez Gene ID
57127
Genome
hg19
Position
chr1:156,339,002-156,355,011
Genome
hg38
Position
chr1:156,369,211-156,385,219
MIM
607079 OMIM
HGNC
HGNC:14572 HGNC
Ensembl
ENSG00000132677 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 62
Ranking
ClinVar
0
0
0
64
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 SLC42A2
MIM 607079 OMIM
HGNC HGNC:14572 HGNC
Ensembl ENSG00000132677 Ensembl
AllianceGenome HGNC:14572
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000537040.6 hg38 chr1 156,369,211 156,385,219 16,009
ENST00000537040.6 hg19 chr1 156,339,002 156,355,011 16,010
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