Canonical Allele Identifier: CA1882582387
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257502A= , CM000671.2:g.133257502A= GRCh38
NC_000009.11:g.136132889A= , CM000671.1:g.136132889A= GRCh37
NC_000009.10:g.135122710A= NCBI36
NG_006669.1:g.20166T=
NG_006669.2:g.22714T=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.310T=
ENST00000647353.1:n.54-6350T=
ENST00000651471.1:n.329+540T=
ENST00000679909.1:c.28+17660T= ENSP00000506089.1:n.28+17660T=
ENST00000453660.3:n.292T=
ENST00000538324.2:c.278T= ENSP00000483018.1:p.Ile93=
ENST00000611156.4:c.278T= ENSP00000483265.1:p.Ile93=
NM_020469.2:c.281T= NP_065202.2:p.Ile94=
NM_020469.3:c.281T= NP_065202.2:p.Ile94=