Canonical Allele Identifier: CA1882579989
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255954G= , CM000671.2:g.133255954G= GRCh38
NC_000009.11:g.136131341G= , CM000671.1:g.136131341G= GRCh37
NC_000009.10:g.135121162G= NCBI36
NG_006669.1:g.21714C=
NG_006669.2:g.24262C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.806C=
ENST00000647353.1:n.54-4802C=
ENST00000679909.1:c.28+19208C= ENSP00000506089.1:n.28+19208C=
ENST00000453660.3:n.788C=
ENST00000538324.2:c.774C= ENSP00000483018.1:p.Asp258=
ENST00000611156.4:c.774C= ENSP00000483265.1:p.Asp258=
NM_020469.2:c.777C= NP_065202.2:p.Asp259=
NM_020469.3:c.777C= NP_065202.2:p.Asp259=