Canonical Allele Identifier: CA364403754

Gene: RHAG

Linked Data

• dbSNP Id: rs1438746046
• MyVariant Identifiers: chr6:g.49587059A>C (hg19) ; chr6:g.49619346A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619346A>C , CM000668.2:g.49619346A>C	GRCh38
NC_000006.11:g.49587059A>C , CM000668.1:g.49587059A>C	GRCh37
NC_000006.10:g.49695018A>C	NCBI36
NG_011704.1:g.22529T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.174T>G MANE Select	ENSP00000360217.4:p.His58Gln
ENST00000642530.1:n.449T>G
ENST00000646272.1:c.174T>G	ENSP00000494337.1:p.His58Gln
ENST00000646939.1:c.174T>G	ENSP00000494709.1:p.His58Gln
ENST00000646963.1:c.174T>G	ENSP00000495337.1:p.His58Gln
ENST00000229810.9:c.174T>G	ENSP00000229810.8:p.His58Gln
ENST00000371175.8:c.174T>G	ENSP00000360217.4:p.His58Gln
ENST00000618248.3:c.174T>G	ENSP00000482984.1:p.His58Gln
NM_000324.2:c.174T>G	NP_000315.2:p.His58Gln
XM_011514788.1:c.174T>G	XP_011513090.1:p.His58Gln
NM_000324.3:c.174T>G MANE Select	NP_000315.2:p.His58Gln