Canonical Allele Identifier: CA1882580294
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256083G= , CM000671.2:g.133256083G= GRCh38
NC_000009.11:g.136131470G= , CM000671.1:g.136131470G= GRCh37
NC_000009.10:g.135121291G= NCBI36
NG_006669.1:g.21585C=
NG_006669.2:g.24133C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.677C=
ENST00000647353.1:n.54-4931C=
ENST00000679909.1:c.28+19079C= ENSP00000506089.1:n.28+19079C=
ENST00000453660.3:n.659C=
ENST00000538324.2:c.645C= ENSP00000483018.1:p.Phe215=
ENST00000611156.4:c.645C= ENSP00000483265.1:p.Phe215=
NM_020469.2:c.648C= NP_065202.2:p.Phe216=
NM_020469.3:c.648C= NP_065202.2:p.Phe216=