Canonical Allele Identifier: CA1882579239
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255672G= , CM000671.2:g.133255672G= GRCh38
NC_000009.11:g.136131059G= , CM000671.1:g.136131059G= GRCh37
NC_000009.10:g.135120880G= NCBI36
NG_006669.1:g.21996C=
NG_006669.2:g.24544C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1088C=
ENST00000647353.1:n.54-4520C=
ENST00000679909.1:c.28+19490C= ENSP00000506089.1:n.28+19490C=
ENST00000453660.3:n.1070C=
ENST00000538324.2:c.1054-2C= ENSP00000483018.1:n.1054-2C=
ENST00000611156.4:c.1056C= ENSP00000483265.1:p.Asn352=
NM_020469.2:c.1059C= NP_065202.2:p.Asn353=
NM_020469.3:c.1059C= NP_065202.2:p.Asn353=