Canonical Allele Identifier: CA1882582304
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257450G= , CM000671.2:g.133257450G= GRCh38
NC_000009.11:g.136132837G= , CM000671.1:g.136132837G= GRCh37
NC_000009.10:g.135122658G= NCBI36
NG_006669.1:g.20218C=
NG_006669.2:g.22766C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.362C=
ENST00000647353.1:n.54-6298C=
ENST00000651471.1:n.329+592C=
ENST00000679909.1:c.28+17712C= ENSP00000506089.1:n.28+17712C=
ENST00000453660.3:n.344C=
ENST00000538324.2:c.330C= ENSP00000483018.1:p.Leu110=
ENST00000611156.4:c.330C= ENSP00000483265.1:p.Leu110=
NM_020469.2:c.333C= NP_065202.2:p.Leu111=
NM_020469.3:c.333C= NP_065202.2:p.Leu111=