Canonical Allele Identifier: CA1882579415
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255746G= , CM000671.2:g.133255746G= GRCh38
NC_000009.11:g.136131133G= , CM000671.1:g.136131133G= GRCh37
NC_000009.10:g.135120954G= NCBI36
NG_006669.1:g.21922C=
NG_006669.2:g.24470C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1014C=
ENST00000647353.1:n.54-4594C=
ENST00000679909.1:c.28+19416C= ENSP00000506089.1:n.28+19416C=
ENST00000453660.3:n.996C=
ENST00000538324.2:c.982C= ENSP00000483018.1:p.Leu328=
ENST00000611156.4:c.982C= ENSP00000483265.1:p.Leu328=
NM_020469.2:c.985C= NP_065202.2:p.Leu329=
NM_020469.3:c.985C= NP_065202.2:p.Leu329=