Canonical Allele Identifier: CA567156171

Gene: RHAG

Linked Data

• dbSNP Id: rs1221396309
• gnomAD v2: 6-49587098-AT-A
• gnomAD v4: 6-49619385-AT-A
• MyVariant Identifiers: chr6:g.49587099del (hg19) ; chr6:g.49619386del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619386del , CM000668.2:g.49619386del	GRCh38
NC_000006.11:g.49587099del , CM000668.1:g.49587099del	GRCh37
NC_000006.10:g.49695058del	NCBI36
NG_011704.1:g.22489del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.158-24del MANE Select	ENSP00000360217.4:n.158-24del
ENST00000642530.1:n.433-24del
ENST00000646272.1:c.158-24del	ENSP00000494337.1:n.158-24del
ENST00000646939.1:c.158-24del	ENSP00000494709.1:n.158-24del
ENST00000646963.1:c.158-24del	ENSP00000495337.1:n.158-24del
ENST00000229810.9:c.158-24del	ENSP00000229810.8:n.158-24del
ENST00000371175.8:c.158-24del	ENSP00000360217.4:n.158-24del
ENST00000618248.3:c.158-24del	ENSP00000482984.1:n.158-24del
NM_000324.2:c.158-24del	NP_000315.2:n.158-24del
XM_011514788.1:c.158-24del	XP_011513090.1:n.158-24del
NM_000324.3:c.158-24del MANE Select	NP_000315.2:n.158-24del