Canonical Allele Identifier: CA2679058387

Gene: RHAG

Linked Data

• gnomAD v4: 6-49619447-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619447C>A , CM000668.2:g.49619447C>A	GRCh38
NC_000006.11:g.49587160C>A , CM000668.1:g.49587160C>A	GRCh37
NC_000006.10:g.49695119C>A	NCBI36
NG_011704.1:g.22428G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.158-85G>T MANE Select	ENSP00000360217.4:n.158-85G>T
ENST00000642530.1:n.433-85G>T
ENST00000646272.1:c.158-85G>T	ENSP00000494337.1:n.158-85G>T
ENST00000646939.1:c.158-85G>T	ENSP00000494709.1:n.158-85G>T
ENST00000646963.1:c.158-85G>T	ENSP00000495337.1:n.158-85G>T
ENST00000229810.9:c.158-85G>T	ENSP00000229810.8:n.158-85G>T
ENST00000371175.8:c.158-85G>T	ENSP00000360217.4:n.158-85G>T
ENST00000618248.3:c.158-85G>T	ENSP00000482984.1:n.158-85G>T
NM_000324.2:c.158-85G>T	NP_000315.2:n.158-85G>T
XM_011514788.1:c.158-85G>T	XP_011513090.1:n.158-85G>T
NM_000324.3:c.158-85G>T MANE Select	NP_000315.2:n.158-85G>T