Canonical Allele Identifier: CA364398115

Gene: RHAG

Linked Data

• MyVariant Identifiers: chr6:g.49580119C>A (hg19) ; chr6:g.49612406C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49612406C>A , CM000668.2:g.49612406C>A	GRCh38
NC_000006.11:g.49580119C>A , CM000668.1:g.49580119C>A	GRCh37
NC_000006.10:g.49688078C>A	NCBI36
NG_011704.1:g.29469G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371175.10:c.936G>T MANE Select	ENSP00000360217.4:p.Lys312Asn
ENST00000646272.1:c.936G>T	ENSP00000494337.1:p.Lys312Asn
ENST00000646939.1:c.936G>T	ENSP00000494709.1:p.Lys312Asn
ENST00000646963.1:c.936G>T	ENSP00000495337.1:p.Lys312Asn
ENST00000229810.9:c.936G>T	ENSP00000229810.8:p.Lys312Asn
ENST00000371175.8:c.936G>T	ENSP00000360217.4:p.Lys312Asn
ENST00000618248.3:c.936G>T	ENSP00000482984.1:p.Lys312Asn
NM_000324.2:c.936G>T	NP_000315.2:p.Lys312Asn
NM_000324.3:c.936G>T MANE Select	NP_000315.2:p.Lys312Asn