Canonical Allele Identifier: CA653752352

Gene: ABO

Linked Data

• COSMIC: COSN23036762 ; COSN23184073 ; COSN23220511

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255416_133255417insGT , CM000671.2:g.133255416_133255417insGT	GRCh38
NC_000009.11:g.136130803_136130804insGT , CM000671.1:g.136130803_136130804insGT	GRCh37
NC_000009.10:g.135120624_135120625insGT	NCBI36
NG_006669.1:g.22251_22252insAC
NG_006669.2:g.24799_24800insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1343_1344insAC
ENST00000647353.1:n.54-4265_54-4264insAC
ENST00000679909.1:c.28+19745_28+19746insAC	ENSP00000506089.1:n.28+19745_28+19746insAC
ENST00000453660.3:n.1325_1326insAC
ENST00000611156.4:c.*249_*250insAC	ENSP00000483265.1:n.*249_*250insAC
NM_020469.2:c.*249_*250insAC	NP_065202.2:n.*249_*250insAC
NM_020469.3:c.*249_*250insAC	NP_065202.2:n.*249_*250insAC