Canonical Allele Identifier: CA1882582768
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257791G= , CM000671.2:g.133257791G= GRCh38
NC_000009.11:g.136133178G= , CM000671.1:g.136133178G= GRCh37
NC_000009.10:g.135122999G= NCBI36
NG_006669.1:g.19876C=
NG_006669.2:g.22424C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-249C=
ENST00000647353.1:n.54-6639C=
ENST00000651471.1:n.329+251C=
ENST00000679909.1:c.28+17371C= ENSP00000506089.1:n.28+17371C=
ENST00000453660.3:n.252-249C=
ENST00000538324.2:c.240-249C= ENSP00000483018.1:n.240-249C=
ENST00000611156.4:c.240-249C= ENSP00000483265.1:n.240-249C=
NM_020469.2:c.240-249C= NP_065202.2:n.240-249C=
NM_020469.3:c.240-249C= NP_065202.2:n.240-249C=