Canonical Allele Identifier: CA364398172

Gene: RHAG

Linked Data

• MyVariant Identifiers: chr6:g.49580132A>T (hg19) ; chr6:g.49612419A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49612419A>T , CM000668.2:g.49612419A>T	GRCh38
NC_000006.11:g.49580132A>T , CM000668.1:g.49580132A>T	GRCh37
NC_000006.10:g.49688091A>T	NCBI36
NG_011704.1:g.29456T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.923T>A MANE Select	ENSP00000360217.4:p.Val308Glu
ENST00000646272.1:c.923T>A	ENSP00000494337.1:p.Val308Glu
ENST00000646874.1:n.613T>A
ENST00000646939.1:c.923T>A	ENSP00000494709.1:p.Val308Glu
ENST00000646963.1:c.923T>A	ENSP00000495337.1:p.Val308Glu
ENST00000229810.9:c.923T>A	ENSP00000229810.8:p.Val308Glu
ENST00000371175.8:c.923T>A	ENSP00000360217.4:p.Val308Glu
ENST00000618248.3:c.923T>A	ENSP00000482984.1:p.Val308Glu
NM_000324.2:c.923T>A	NP_000315.2:p.Val308Glu
NM_000324.3:c.923T>A MANE Select	NP_000315.2:p.Val308Glu