Canonical Allele Identifier: CA1882580003
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255960G= , CM000671.2:g.133255960G= GRCh38
NC_000009.11:g.136131347G= , CM000671.1:g.136131347G= GRCh37
NC_000009.10:g.135121168G= NCBI36
NG_006669.1:g.21708C=
NG_006669.2:g.24256C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.800C=
ENST00000647353.1:n.54-4808C=
ENST00000679909.1:c.28+19202C= ENSP00000506089.1:n.28+19202C=
ENST00000453660.3:n.782C=
ENST00000538324.2:c.768C= ENSP00000483018.1:p.Pro256=
ENST00000611156.4:c.768C= ENSP00000483265.1:p.Pro256=
NM_020469.2:c.771C= NP_065202.2:p.Pro257=
NM_020469.3:c.771C= NP_065202.2:p.Pro257=