Canonical Allele Identifier: CA2840263418
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258076A>G , CM000671.2:g.133258076A>G GRCh38
NC_000009.11:g.136133466A>G , CM000671.1:g.136133466A>G GRCh37
NC_000009.10:g.135123287A>G NCBI36
NG_006669.1:g.19588T>C
NG_006669.2:g.22139T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+21T>C
ENST00000647353.1:n.54-6924T>C
ENST00000651471.1:n.295T>C
ENST00000679909.1:c.28+17086T>C ENSP00000506089.1:n.28+17086T>C
ENST00000453660.3:n.251+21T>C
ENST00000538324.2:c.239+21T>C ENSP00000483018.1:n.239+21T>C
ENST00000611156.4:c.239+21T>C ENSP00000483265.1:n.239+21T>C
NM_020469.2:c.239+21T>C NP_065202.2:n.239+21T>C
NM_020469.3:c.239+21T>C NP_065202.2:n.239+21T>C