Canonical Allele Identifier: CA2580907973
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257138T>A , CM000671.2:g.133257138T>A GRCh38
NC_000009.11:g.136132525T>A , CM000671.1:g.136132525T>A GRCh37
NC_000009.10:g.135122346T>A NCBI36
NG_006669.1:g.20530A>T
NG_006669.2:g.23078A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+271A>T
ENST00000647353.1:n.54-5986A>T
ENST00000651471.1:n.330-782A>T
ENST00000679909.1:c.28+18024A>T ENSP00000506089.1:n.28+18024A>T
ENST00000453660.3:n.385+271A>T
ENST00000538324.2:c.371+271A>T ENSP00000483018.1:n.371+271A>T
ENST00000611156.4:c.371+271A>T ENSP00000483265.1:n.371+271A>T
NM_020469.2:c.374+271A>T NP_065202.2:n.374+271A>T
NM_020469.3:c.374+271A>T NP_065202.2:n.374+271A>T