Canonical Allele Identifier: CA1882580813
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256264G= , CM000671.2:g.133256264G= GRCh38
NC_000009.11:g.136131651G= , CM000671.1:g.136131651G= GRCh37
NC_000009.10:g.135121472G= NCBI36
NG_006669.1:g.21404C=
NG_006669.2:g.23952C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.496C=
ENST00000647353.1:n.54-5112C=
ENST00000651471.1:n.422C=
ENST00000679909.1:c.28+18898C= ENSP00000506089.1:n.28+18898C=
ENST00000453660.3:n.478C=
ENST00000538324.2:c.464C= ENSP00000483018.1:p.Pro155=
ENST00000611156.4:c.464C= ENSP00000483265.1:p.Pro155=
NM_020469.2:c.467C= NP_065202.2:p.Pro156=
NM_020469.3:c.467C= NP_065202.2:p.Pro156=