Canonical Allele Identifier: CA1882582782
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834630568

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257802G>A , CM000671.2:g.133257802G>A GRCh38
NC_000009.11:g.136133189G>A , CM000671.1:g.136133189G>A GRCh37
NC_000009.10:g.135123010G>A NCBI36
NG_006669.1:g.19865C>T
NG_006669.2:g.22413C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-260C>T
ENST00000647353.1:n.54-6650C>T
ENST00000651471.1:n.329+240C>T
ENST00000679909.1:c.28+17360C>T ENSP00000506089.1:n.28+17360C>T
ENST00000453660.3:n.252-260C>T
ENST00000538324.2:c.240-260C>T ENSP00000483018.1:n.240-260C>T
ENST00000611156.4:c.240-260C>T ENSP00000483265.1:n.240-260C>T
NM_020469.2:c.240-260C>T NP_065202.2:n.240-260C>T
NM_020469.3:c.240-260C>T NP_065202.2:n.240-260C>T