Canonical Allele Identifier: CA1882580480
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256152A= , CM000671.2:g.133256152A= GRCh38
NC_000009.11:g.136131539A= , CM000671.1:g.136131539A= GRCh37
NC_000009.10:g.135121360A= NCBI36
NG_006669.1:g.21516T=
NG_006669.2:g.24064T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.608T=
ENST00000647353.1:n.54-5000T=
ENST00000651471.1:n.534T=
ENST00000679909.1:c.28+19010T= ENSP00000506089.1:n.28+19010T=
ENST00000453660.3:n.590T=
ENST00000538324.2:c.576T= ENSP00000483018.1:p.Ser192=
ENST00000611156.4:c.576T= ENSP00000483265.1:p.Ser192=
NM_020469.2:c.579T= NP_065202.2:p.Ser193=
NM_020469.3:c.579T= NP_065202.2:p.Ser193=