Canonical Allele Identifier: CA1627477908

Gene: RHAG

Linked Data

• dbSNP Id: rs1762707250
• gnomAD v4: 6-49619116-T-TTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619117_49619118dup , CM000668.2:g.49619117_49619118dup	GRCh38
NC_000006.11:g.49586830_49586831dup , CM000668.1:g.49586830_49586831dup	GRCh37
NC_000006.10:g.49694789_49694790dup	NCBI36
NG_011704.1:g.22757_22758dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.341+61_341+62dup MANE Select	ENSP00000360217.4:n.341+61_341+62dup
ENST00000642530.1:n.616+61_616+62dup
ENST00000646272.1:c.341+61_341+62dup	ENSP00000494337.1:n.341+61_341+62dup
ENST00000646939.1:c.341+61_341+62dup	ENSP00000494709.1:n.341+61_341+62dup
ENST00000646963.1:c.341+61_341+62dup	ENSP00000495337.1:n.341+61_341+62dup
ENST00000229810.9:c.341+61_341+62dup	ENSP00000229810.8:n.341+61_341+62dup
ENST00000371175.8:c.341+61_341+62dup	ENSP00000360217.4:n.341+61_341+62dup
ENST00000618248.3:c.341+61_341+62dup	ENSP00000482984.1:n.341+61_341+62dup
NM_000324.2:c.341+61_341+62dup	NP_000315.2:n.341+61_341+62dup
XM_011514788.1:c.341+61_341+62dup	XP_011513090.1:n.341+61_341+62dup
NM_000324.3:c.341+61_341+62dup MANE Select	NP_000315.2:n.341+61_341+62dup