Canonical Allele Identifier: CA2679055067
Gene: RHAG HGNC NCBI

Linked Data

gnomAD v4: 6-49636837-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49636837A>G , CM000668.2:g.49636837A>G GRCh38
NC_000006.11:g.49604550A>G , CM000668.1:g.49604550A>G GRCh37
NC_000006.10:g.49712509A>G NCBI36
NG_011704.1:g.5038T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371175.10:c.-25T>C MANE Select ENSP00000360217.4:n.-25T>C
ENST00000642530.1:n.3T>C
ENST00000646272.1:c.-25T>C ENSP00000494337.1:n.-25T>C
ENST00000646939.1:c.-25T>C ENSP00000494709.1:n.-25T>C
ENST00000646963.1:c.-25T>C ENSP00000495337.1:n.-25T>C
ENST00000229810.9:c.-25T>C ENSP00000229810.8:n.-25T>C
ENST00000371175.8:c.-25T>C ENSP00000360217.4:n.-25T>C
ENST00000618248.3:c.-25T>C ENSP00000482984.1:n.-25T>C
NM_000324.2:c.-25T>C NP_000315.2:n.-25T>C
XM_011514788.1:c.-25T>C XP_011513090.1:n.-25T>C
NM_000324.3:c.-25T>C MANE Select NP_000315.2:n.-25T>C
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