Canonical Allele Identifier: CA364403269
Gene: RHAG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49619263A>T , CM000668.2:g.49619263A>T GRCh38
NC_000006.11:g.49586976A>T , CM000668.1:g.49586976A>T GRCh37
NC_000006.10:g.49694935A>T NCBI36
NG_011704.1:g.22612T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371175.10:c.257T>A MANE Select ENSP00000360217.4:p.Val86Asp
ENST00000642530.1:n.532T>A
ENST00000646272.1:c.257T>A ENSP00000494337.1:p.Val86Asp
ENST00000646939.1:c.257T>A ENSP00000494709.1:p.Val86Asp
ENST00000646963.1:c.257T>A ENSP00000495337.1:p.Val86Asp
ENST00000229810.9:c.257T>A ENSP00000229810.8:p.Val86Asp
ENST00000371175.8:c.257T>A ENSP00000360217.4:p.Val86Asp
ENST00000618248.3:c.257T>A ENSP00000482984.1:p.Val86Asp
NM_000324.2:c.257T>A NP_000315.2:p.Val86Asp
XM_011514788.1:c.257T>A XP_011513090.1:p.Val86Asp
NM_000324.3:c.257T>A MANE Select NP_000315.2:p.Val86Asp