Canonical Allele Identifier: CA2786163905
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274153T>A , CM000671.2:g.133274153T>A GRCh38
NC_000009.11:g.136149569T>A , CM000671.1:g.136149569T>A GRCh37
NC_000009.10:g.135139390T>A NCBI36
NG_006669.1:g.3482A>T
NG_006669.2:g.6062A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.58+1009A>T
ENST00000647353.1:n.53+1009A>T
ENST00000651471.1:n.63+1809A>T
ENST00000679909.1:c.28+1009A>T ENSP00000506089.1:n.28+1009A>T
ENST00000453660.3:n.40+1009A>T
ENST00000538324.2:c.28+1009A>T ENSP00000483018.1:n.28+1009A>T
ENST00000611156.4:c.28+1009A>T ENSP00000483265.1:n.28+1009A>T
NM_020469.2:c.28+1009A>T NP_065202.2:n.28+1009A>T
NM_020469.3:c.28+1009A>T NP_065202.2:n.28+1009A>T