Canonical Allele Identifier: CA1882580915
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256311G= , CM000671.2:g.133256311G= GRCh38
NC_000009.11:g.136131698G= , CM000671.1:g.136131698G= GRCh37
NC_000009.10:g.135121519G= NCBI36
NG_006669.1:g.21357C=
NG_006669.2:g.23905C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.449C=
ENST00000647353.1:n.54-5159C=
ENST00000651471.1:n.375C=
ENST00000679909.1:c.28+18851C= ENSP00000506089.1:n.28+18851C=
ENST00000453660.3:n.431C=
ENST00000538324.2:c.417C= ENSP00000483018.1:p.His139=
ENST00000611156.4:c.417C= ENSP00000483265.1:p.His139=
NM_020469.2:c.420C= NP_065202.2:p.His140=
NM_020469.3:c.420C= NP_065202.2:p.His140=