Canonical Allele Identifier: CA1882579671
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255845T= , CM000671.2:g.133255845T= GRCh38
NC_000009.11:g.136131232T= , CM000671.1:g.136131232T= GRCh37
NC_000009.10:g.135121053T= NCBI36
NG_006669.1:g.21823A=
NG_006669.2:g.24371A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.915A=
ENST00000647353.1:n.54-4693A=
ENST00000679909.1:c.28+19317A= ENSP00000506089.1:n.28+19317A=
ENST00000453660.3:n.897A=
ENST00000538324.2:c.883A= ENSP00000483018.1:p.Ile295=
ENST00000611156.4:c.883A= ENSP00000483265.1:p.Ile295=
NM_020469.2:c.886A= NP_065202.2:p.Ile296=
NM_020469.3:c.886A= NP_065202.2:p.Ile296=