Canonical Allele Identifier: CA3847961
Gene: RHAG HGNC NCBI

Linked Data

dbSNP Id: rs765698136
gnomAD v2: 6-49586999-G-A
gnomAD v4: 6-49619286-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49619286G>A , CM000668.2:g.49619286G>A GRCh38
NC_000006.11:g.49586999G>A , CM000668.1:g.49586999G>A GRCh37
NC_000006.10:g.49694958G>A NCBI36
NG_011704.1:g.22589C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371175.10:c.234C>T MANE Select ENSP00000360217.4:p.Ser78=
ENST00000642530.1:n.509C>T
ENST00000646272.1:c.234C>T ENSP00000494337.1:p.Ser78=
ENST00000646939.1:c.234C>T ENSP00000494709.1:p.Ser78=
ENST00000646963.1:c.234C>T ENSP00000495337.1:p.Ser78=
ENST00000229810.9:c.234C>T ENSP00000229810.8:p.Ser78=
ENST00000371175.8:c.234C>T ENSP00000360217.4:p.Ser78=
ENST00000618248.3:c.234C>T ENSP00000482984.1:p.Ser78=
NM_000324.2:c.234C>T NP_000315.2:p.Ser78=
XM_011514788.1:c.234C>T XP_011513090.1:p.Ser78=
NM_000324.3:c.234C>T MANE Select NP_000315.2:p.Ser78=