Canonical Allele Identifier: CA450402616

Gene: RHAG

Linked Data

• gnomAD v4: 6-49619280-C-A
• MyVariant Identifiers: chr6:g.49586993C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619280C>A , CM000668.2:g.49619280C>A	GRCh38
NC_000006.11:g.49586993C>A , CM000668.1:g.49586993C>A	GRCh37
NC_000006.10:g.49694952C>A	NCBI36
NG_011704.1:g.22595G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.240G>T MANE Select	ENSP00000360217.4:p.Val80=
ENST00000642530.1:n.515G>T
ENST00000646272.1:c.240G>T	ENSP00000494337.1:p.Val80=
ENST00000646939.1:c.240G>T	ENSP00000494709.1:p.Val80=
ENST00000646963.1:c.240G>T	ENSP00000495337.1:p.Val80=
ENST00000229810.9:c.240G>T	ENSP00000229810.8:p.Val80=
ENST00000371175.8:c.240G>T	ENSP00000360217.4:p.Val80=
ENST00000618248.3:c.240G>T	ENSP00000482984.1:p.Val80=
NM_000324.2:c.240G>T	NP_000315.2:p.Val80=
XM_011514788.1:c.240G>T	XP_011513090.1:p.Val80=
NM_000324.3:c.240G>T MANE Select	NP_000315.2:p.Val80=