Canonical Allele Identifier: CA3847786

Gene: RHAG

Linked Data

• dbSNP Id: rs563253807
• ExAC: 6:49580122 G / A
• gnomAD v2: 6-49580122-G-A
• gnomAD v3: 6-49612409-G-A
• gnomAD v4: 6-49612409-G-A
• MyVariant Identifiers: chr6:g.49580122G>A (hg19) ; chr6:g.49612409G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49612409G>A , CM000668.2:g.49612409G>A	GRCh38
NC_000006.11:g.49580122G>A , CM000668.1:g.49580122G>A	GRCh37
NC_000006.10:g.49688081G>A	NCBI36
NG_011704.1:g.29466C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371175.10:c.933C>T MANE Select	ENSP00000360217.4:p.Tyr311=
ENST00000646272.1:c.933C>T	ENSP00000494337.1:p.Tyr311=
ENST00000646874.1:n.623C>T
ENST00000646939.1:c.933C>T	ENSP00000494709.1:p.Tyr311=
ENST00000646963.1:c.933C>T	ENSP00000495337.1:p.Tyr311=
ENST00000229810.9:c.933C>T	ENSP00000229810.8:p.Tyr311=
ENST00000371175.8:c.933C>T	ENSP00000360217.4:p.Tyr311=
ENST00000618248.3:c.933C>T	ENSP00000482984.1:p.Tyr311=
NM_000324.2:c.933C>T	NP_000315.2:p.Tyr311=
NM_000324.3:c.933C>T MANE Select	NP_000315.2:p.Tyr311=