Canonical Allele Identifier: CA1882585051
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261685G= , CM000671.2:g.133261685G= GRCh38
NC_000009.11:g.136137088G= , CM000671.1:g.136137088G= GRCh37
NC_000009.10:g.135126909G= NCBI36
NG_006669.1:g.15965C=
NG_006669.2:g.18530C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.129-311C=
ENST00000647353.1:n.54-10533C=
ENST00000651471.1:n.134-311C=
ENST00000679909.1:c.28+13477C= ENSP00000506089.1:n.28+13477C=
ENST00000453660.3:n.111-311C=
ENST00000538324.2:c.99-311C= ENSP00000483018.1:n.99-311C=
ENST00000611156.4:c.99-311C= ENSP00000483265.1:n.99-311C=
NM_020469.2:c.99-311C= NP_065202.2:n.99-311C=
NM_020469.3:c.99-311C= NP_065202.2:n.99-311C=