Canonical Allele Identifier: CA1882582674
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257712G= , CM000671.2:g.133257712G= GRCh38
NC_000009.11:g.136133099G= , CM000671.1:g.136133099G= GRCh37
NC_000009.10:g.135122920G= NCBI36
NG_006669.1:g.19955C=
NG_006669.2:g.22503C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-170C=
ENST00000647353.1:n.54-6560C=
ENST00000651471.1:n.329+330C=
ENST00000679909.1:c.28+17450C= ENSP00000506089.1:n.28+17450C=
ENST00000453660.3:n.252-170C=
ENST00000538324.2:c.240-170C= ENSP00000483018.1:n.240-170C=
ENST00000611156.4:c.240-170C= ENSP00000483265.1:n.240-170C=
NM_020469.2:c.240-170C= NP_065202.2:n.240-170C=
NM_020469.3:c.240-170C= NP_065202.2:n.240-170C=