Canonical Allele Identifier: CA1882579492
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255772G= , CM000671.2:g.133255772G= GRCh38
NC_000009.11:g.136131159G= , CM000671.1:g.136131159G= GRCh37
NC_000009.10:g.135120980G= NCBI36
NG_006669.1:g.21896C=
NG_006669.2:g.24444C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.988C=
ENST00000647353.1:n.54-4620C=
ENST00000679909.1:c.28+19390C= ENSP00000506089.1:n.28+19390C=
ENST00000453660.3:n.970C=
ENST00000538324.2:c.956C= ENSP00000483018.1:p.Ser319=
ENST00000611156.4:c.956C= ENSP00000483265.1:p.Ser319=
NM_020469.2:c.959C= NP_065202.2:p.Ser320=
NM_020469.3:c.959C= NP_065202.2:p.Ser320=