Canonical Allele Identifier: CA1882579088
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255619A= , CM000671.2:g.133255619A= GRCh38
NC_000009.11:g.136131006A= , CM000671.1:g.136131006A= GRCh37
NC_000009.10:g.135120827A= NCBI36
NG_006669.1:g.22049T=
NG_006669.2:g.24597T=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1141T=
ENST00000647353.1:n.54-4467T=
ENST00000679909.1:c.28+19543T= ENSP00000506089.1:n.28+19543T=
ENST00000453660.3:n.1123T=
ENST00000538324.2:c.1105T= ENSP00000483018.1:p.Ser369=
ENST00000611156.4:c.*47T= ENSP00000483265.1:n.*47T=
NM_020469.2:c.*47T= NP_065202.2:n.*47T=
NM_020469.3:c.*47T= NP_065202.2:n.*47T=