Canonical Allele Identifier: CA450399490

Gene: RHAG

Linked Data

• MyVariant Identifiers: chr6:g.49604505G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49636792G>T , CM000668.2:g.49636792G>T	GRCh38
NC_000006.11:g.49604505G>T , CM000668.1:g.49604505G>T	GRCh37
NC_000006.10:g.49712464G>T	NCBI36
NG_011704.1:g.5083C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.21C>A MANE Select	ENSP00000360217.4:p.Leu7=
ENST00000642530.1:n.48C>A
ENST00000646272.1:c.21C>A	ENSP00000494337.1:p.Leu7=
ENST00000646939.1:c.21C>A	ENSP00000494709.1:p.Leu7=
ENST00000646963.1:c.21C>A	ENSP00000495337.1:p.Leu7=
ENST00000229810.9:c.21C>A	ENSP00000229810.8:p.Leu7=
ENST00000371175.8:c.21C>A	ENSP00000360217.4:p.Leu7=
ENST00000618248.3:c.21C>A	ENSP00000482984.1:p.Leu7=
NM_000324.2:c.21C>A	NP_000315.2:p.Leu7=
XM_011514788.1:c.21C>A	XP_011513090.1:p.Leu7=
NM_000324.3:c.21C>A MANE Select	NP_000315.2:p.Leu7=