Canonical Allele Identifier: CA1882579993
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255955T= , CM000671.2:g.133255955T= GRCh38
NC_000009.11:g.136131342T= , CM000671.1:g.136131342T= GRCh37
NC_000009.10:g.135121163T= NCBI36
NG_006669.1:g.21713A=
NG_006669.2:g.24261A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.805A=
ENST00000647353.1:n.54-4803A=
ENST00000679909.1:c.28+19207A= ENSP00000506089.1:n.28+19207A=
ENST00000453660.3:n.787A=
ENST00000538324.2:c.773A= ENSP00000483018.1:p.Asp258=
ENST00000611156.4:c.773A= ENSP00000483265.1:p.Asp258=
NM_020469.2:c.776A= NP_065202.2:p.Asp259=
NM_020469.3:c.776A= NP_065202.2:p.Asp259=