Canonical Allele Identifier: CA2786163305
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257732T>G , CM000671.2:g.133257732T>G GRCh38
NC_000009.11:g.136133119T>G , CM000671.1:g.136133119T>G GRCh37
NC_000009.10:g.135122940T>G NCBI36
NG_006669.1:g.19935A>C
NG_006669.2:g.22483A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-190A>C
ENST00000647353.1:n.54-6580A>C
ENST00000651471.1:n.329+310A>C
ENST00000679909.1:c.28+17430A>C ENSP00000506089.1:n.28+17430A>C
ENST00000453660.3:n.252-190A>C
ENST00000538324.2:c.240-190A>C ENSP00000483018.1:n.240-190A>C
ENST00000611156.4:c.240-190A>C ENSP00000483265.1:n.240-190A>C
NM_020469.2:c.240-190A>C NP_065202.2:n.240-190A>C
NM_020469.3:c.240-190A>C NP_065202.2:n.240-190A>C