Canonical Allele Identifier: CA2786163310
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257879T>A , CM000671.2:g.133257879T>A GRCh38
NC_000009.11:g.136133266T>A , CM000671.1:g.136133266T>A GRCh37
NC_000009.10:g.135123087T>A NCBI36
NG_006669.1:g.19788A>T
NG_006669.2:g.22336A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+218A>T
ENST00000647353.1:n.54-6727A>T
ENST00000651471.1:n.329+163A>T
ENST00000679909.1:c.28+17283A>T ENSP00000506089.1:n.28+17283A>T
ENST00000453660.3:n.251+218A>T
ENST00000538324.2:c.239+218A>T ENSP00000483018.1:n.239+218A>T
ENST00000611156.4:c.239+218A>T ENSP00000483265.1:n.239+218A>T
NM_020469.2:c.239+218A>T NP_065202.2:n.239+218A>T
NM_020469.3:c.239+218A>T NP_065202.2:n.239+218A>T