Canonical Allele Identifier: CA1882580324
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256093T= , CM000671.2:g.133256093T= GRCh38
NC_000009.11:g.136131480T= , CM000671.1:g.136131480T= GRCh37
NC_000009.10:g.135121301T= NCBI36
NG_006669.1:g.21575A=
NG_006669.2:g.24123A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.667A=
ENST00000647353.1:n.54-4941A=
ENST00000679909.1:c.28+19069A= ENSP00000506089.1:n.28+19069A=
ENST00000453660.3:n.649A=
ENST00000538324.2:c.635A= ENSP00000483018.1:p.Asp212=
ENST00000611156.4:c.635A= ENSP00000483265.1:p.Asp212=
NM_020469.2:c.638A= NP_065202.2:p.Asp213=
NM_020469.3:c.638A= NP_065202.2:p.Asp213=