Canonical Allele Identifier: CA1882584340
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260056C= , CM000671.2:g.133260056C= GRCh38
NC_000009.11:g.136135460C= , CM000671.1:g.136135460C= GRCh37
NC_000009.10:g.135125281C= NCBI36
NG_006669.1:g.17594G=
NG_006669.2:g.20159G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.186-190G=
ENST00000647353.1:n.54-8904G=
ENST00000651471.1:n.191-190G=
ENST00000679909.1:c.28+15106G= ENSP00000506089.1:n.28+15106G=
ENST00000453660.3:n.168-190G=
ENST00000538324.2:c.156-190G= ENSP00000483018.1:n.156-190G=
ENST00000611156.4:c.156-190G= ENSP00000483265.1:n.156-190G=
NM_020469.2:c.156-190G= NP_065202.2:n.156-190G=
NM_020469.3:c.156-190G= NP_065202.2:n.156-190G=