Canonical Allele Identifier: CA825489308

Gene: RHAG

Linked Data

• dbSNP Id: rs556159035
• gnomAD v3: 6-49619089-C-G
• gnomAD v4: 6-49619089-C-G
• MyVariant Identifiers: chr6:g.49586802C>G (hg19) ; chr6:g.49619089C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619089C>G , CM000668.2:g.49619089C>G	GRCh38
NC_000006.11:g.49586802C>G , CM000668.1:g.49586802C>G	GRCh37
NC_000006.10:g.49694761C>G	NCBI36
NG_011704.1:g.22786G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.341+90G>C MANE Select	ENSP00000360217.4:n.341+90G>C
ENST00000642530.1:n.616+90G>C
ENST00000646272.1:c.341+90G>C	ENSP00000494337.1:n.341+90G>C
ENST00000646939.1:c.341+90G>C	ENSP00000494709.1:n.341+90G>C
ENST00000646963.1:c.341+90G>C	ENSP00000495337.1:n.341+90G>C
ENST00000229810.9:c.341+90G>C	ENSP00000229810.8:n.341+90G>C
ENST00000371175.8:c.341+90G>C	ENSP00000360217.4:n.341+90G>C
ENST00000618248.3:c.341+90G>C	ENSP00000482984.1:n.341+90G>C
NM_000324.2:c.341+90G>C	NP_000315.2:n.341+90G>C
XM_011514788.1:c.341+90G>C	XP_011513090.1:n.341+90G>C
NM_000324.3:c.341+90G>C MANE Select	NP_000315.2:n.341+90G>C