Canonical Allele Identifier: CA5305673

Gene: ABO

Linked Data

• dbSNP Id: rs551612515
• ExAC: 9:136131154 C / T
• gnomAD v2: 9-136131154-C-T
• gnomAD v3: 9-133255767-C-T
• gnomAD v4: 9-133255767-C-T
• MyVariant Identifiers: chr9:g.136131154C>T (hg19) ; chr9:g.136131154_136131155delinsTG (hg19) ; chr9:g.133255767C>T (hg38) ; chr9:g.133255767_133255768delinsTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255767C>T , CM000671.2:g.133255767C>T	GRCh38
NC_000009.11:g.136131154C>T , CM000671.1:g.136131154C>T	GRCh37
NC_000009.10:g.135120975C>T	NCBI36
NG_006669.1:g.21901G>A
NG_006669.2:g.24449G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.993G>A
ENST00000647353.1:n.54-4615G>A
ENST00000679909.1:c.28+19395G>A	ENSP00000506089.1:n.28+19395G>A
ENST00000453660.3:n.975G>A
ENST00000538324.2:c.961G>A	ENSP00000483018.1:p.Glu321Lys
ENST00000611156.4:c.961G>A	ENSP00000483265.1:p.Glu321Lys
NM_020469.2:c.964G>A	NP_065202.2:p.Glu322Lys
NM_020469.3:c.964G>A	NP_065202.2:p.Glu322Lys