Canonical Allele Identifier: CA1882581018
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256365C= , CM000671.2:g.133256365C= GRCh38
NC_000009.11:g.136131752C= , CM000671.1:g.136131752C= GRCh37
NC_000009.10:g.135121573C= NCBI36
NG_006669.1:g.21303G=
NG_006669.2:g.23851G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.404-9G=
ENST00000647353.1:n.54-5213G=
ENST00000651471.1:n.330-9G=
ENST00000679909.1:c.28+18797G= ENSP00000506089.1:n.28+18797G=
ENST00000453660.3:n.386-9G=
ENST00000538324.2:c.372-9G= ENSP00000483018.1:n.372-9G=
ENST00000611156.4:c.372-9G= ENSP00000483265.1:n.372-9G=
NM_020469.2:c.375-9G= NP_065202.2:n.375-9G=
NM_020469.3:c.375-9G= NP_065202.2:n.375-9G=