Canonical Allele Identifier: CA1882582265
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257414G= , CM000671.2:g.133257414G= GRCh38
NC_000009.11:g.136132801G= , CM000671.1:g.136132801G= GRCh37
NC_000009.10:g.135122622G= NCBI36
NG_006669.1:g.20254C=
NG_006669.2:g.22802C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.398C=
ENST00000647353.1:n.54-6262C=
ENST00000651471.1:n.329+628C=
ENST00000679909.1:c.28+17748C= ENSP00000506089.1:n.28+17748C=
ENST00000453660.3:n.380C=
ENST00000538324.2:c.366C= ENSP00000483018.1:p.Ile122=
ENST00000611156.4:c.366C= ENSP00000483265.1:p.Ile122=
NM_020469.2:c.369C= NP_065202.2:p.Ile123=
NM_020469.3:c.369C= NP_065202.2:p.Ile123=