Canonical Allele Identifier: CA1882582340
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257469A= , CM000671.2:g.133257469A= GRCh38
NC_000009.11:g.136132856A= , CM000671.1:g.136132856A= GRCh37
NC_000009.10:g.135122677A= NCBI36
NG_006669.1:g.20199T=
NG_006669.2:g.22747T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.343T=
ENST00000647353.1:n.54-6317T=
ENST00000651471.1:n.329+573T=
ENST00000679909.1:c.28+17693T= ENSP00000506089.1:n.28+17693T=
ENST00000453660.3:n.325T=
ENST00000538324.2:c.311T= ENSP00000483018.1:p.Leu104=
ENST00000611156.4:c.311T= ENSP00000483265.1:p.Leu104=
NM_020469.2:c.314T= NP_065202.2:p.Leu105=
NM_020469.3:c.314T= NP_065202.2:p.Leu105=