Canonical Allele Identifier: CA1882583003
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258072T= , CM000671.2:g.133258072T= GRCh38
NC_000009.11:g.136133462T= , CM000671.1:g.136133462T= GRCh37
NC_000009.10:g.135123283T= NCBI36
NG_006669.1:g.19592A=
NG_006669.2:g.22143A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+25A=
ENST00000647353.1:n.54-6920A=
ENST00000651471.1:n.299A=
ENST00000679909.1:c.28+17090A= ENSP00000506089.1:n.28+17090A=
ENST00000453660.3:n.251+25A=
ENST00000538324.2:c.239+25A= ENSP00000483018.1:n.239+25A=
ENST00000611156.4:c.239+25A= ENSP00000483265.1:n.239+25A=
NM_020469.2:c.239+25A= NP_065202.2:n.239+25A=
NM_020469.3:c.239+25A= NP_065202.2:n.239+25A=