Canonical Allele Identifier: CA1882585044
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261673C= , CM000671.2:g.133261673C= GRCh38
NC_000009.11:g.136137076C= , CM000671.1:g.136137076C= GRCh37
NC_000009.10:g.135126897C= NCBI36
NG_006669.1:g.15977G=
NG_006669.2:g.18542G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.129-299G=
ENST00000647353.1:n.54-10521G=
ENST00000651471.1:n.134-299G=
ENST00000679909.1:c.28+13489G= ENSP00000506089.1:n.28+13489G=
ENST00000453660.3:n.111-299G=
ENST00000538324.2:c.99-299G= ENSP00000483018.1:n.99-299G=
ENST00000611156.4:c.99-299G= ENSP00000483265.1:n.99-299G=
NM_020469.2:c.99-299G= NP_065202.2:n.99-299G=
NM_020469.3:c.99-299G= NP_065202.2:n.99-299G=