Canonical Allele Identifier: CA1882582681
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257721_133257722delinsCG , CM000671.2:g.133257721_133257722delinsCG GRCh38
NC_000009.11:g.136133108_136133109delinsCG , CM000671.1:g.136133108_136133109delinsCG GRCh37
NC_000009.10:g.135122929_135122930delinsCG NCBI36
NG_006669.1:g.19945_19946delinsCG
NG_006669.2:g.22493_22494delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-180_270-179delinsCG
ENST00000647353.1:n.54-6570_54-6569delinsCG
ENST00000651471.1:n.329+320_329+321delinsCG
ENST00000679909.1:c.28+17440_28+17441delinsCG ENSP00000506089.1:n.28+17440_28+17441delinsCG
ENST00000453660.3:n.252-180_252-179delinsCG
ENST00000538324.2:c.240-180_240-179delinsCG ENSP00000483018.1:n.240-180_240-179delinsCG
ENST00000611156.4:c.240-180_240-179delinsCG ENSP00000483265.1:n.240-180_240-179delinsCG
NM_020469.2:c.240-180_240-179delinsCG NP_065202.2:n.240-180_240-179delinsCG
NM_020469.3:c.240-180_240-179delinsCG NP_065202.2:n.240-180_240-179delinsCG