Canonical Allele Identifier: CA1882585213
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133262054C= , CM000671.2:g.133262054C= GRCh38
NC_000009.11:g.136137457C= , CM000671.1:g.136137457C= GRCh37
NC_000009.10:g.135127278C= NCBI36
NG_006669.1:g.15595G=
NG_006669.2:g.18161G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.128+45G=
ENST00000647353.1:n.54-10902G=
ENST00000651471.1:n.133+45G=
ENST00000679909.1:c.28+13108G= ENSP00000506089.1:n.28+13108G=
ENST00000453660.3:n.110+45G=
ENST00000538324.2:c.98+45G= ENSP00000483018.1:n.98+45G=
ENST00000611156.4:c.98+45G= ENSP00000483265.1:n.98+45G=
NM_020469.2:c.98+45G= NP_065202.2:n.98+45G=
NM_020469.3:c.98+45G= NP_065202.2:n.98+45G=