Canonical Allele Identifier: CA364398569

Gene: RHAG

Linked Data

• MyVariant Identifiers: chr6:g.49580232C>A (hg19) ; chr6:g.49612519C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49612519C>A , CM000668.2:g.49612519C>A	GRCh38
NC_000006.11:g.49580232C>A , CM000668.1:g.49580232C>A	GRCh37
NC_000006.10:g.49688191C>A	NCBI36
NG_011704.1:g.29356G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371175.10:c.823G>T MANE Select	ENSP00000360217.4:p.Ala275Ser
ENST00000646272.1:c.823G>T	ENSP00000494337.1:p.Ala275Ser
ENST00000646874.1:n.513G>T
ENST00000646939.1:c.823G>T	ENSP00000494709.1:p.Ala275Ser
ENST00000646963.1:c.823G>T	ENSP00000495337.1:p.Ala275Ser
ENST00000229810.9:c.823G>T	ENSP00000229810.8:p.Ala275Ser
ENST00000371175.8:c.823G>T	ENSP00000360217.4:p.Ala275Ser
ENST00000618248.3:c.823G>T	ENSP00000482984.1:p.Ala275Ser
NM_000324.2:c.823G>T	NP_000315.2:p.Ala275Ser
NM_000324.3:c.823G>T MANE Select	NP_000315.2:p.Ala275Ser