Canonical Allele Identifier: CA1882579978
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255951C= , CM000671.2:g.133255951C= GRCh38
NC_000009.11:g.136131338C= , CM000671.1:g.136131338C= GRCh37
NC_000009.10:g.135121159C= NCBI36
NG_006669.1:g.21717G=
NG_006669.2:g.24265G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.809G=
ENST00000647353.1:n.54-4799G=
ENST00000679909.1:c.28+19211G= ENSP00000506089.1:n.28+19211G=
ENST00000453660.3:n.791G=
ENST00000538324.2:c.777G= ENSP00000483018.1:p.Glu259=
ENST00000611156.4:c.777G= ENSP00000483265.1:p.Glu259=
NM_020469.2:c.780G= NP_065202.2:p.Glu260=
NM_020469.3:c.780G= NP_065202.2:p.Glu260=