Canonical Allele Identifier: CA2692330364
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256296dup , CM000671.2:g.133256296dup GRCh38
NC_000009.11:g.136131683dup , CM000671.1:g.136131683dup GRCh37
NC_000009.10:g.135121504dup NCBI36
NG_006669.1:g.21373dup
NG_006669.2:g.23921dup

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.465dup
ENST00000647353.1:n.54-5143dup
ENST00000651471.1:n.391dup
ENST00000679909.1:c.28+18867dup ENSP00000506089.1:n.28+18867dup
ENST00000453660.3:n.447dup
ENST00000538324.2:c.433dup ENSP00000483018.1:p.Arg145ProfsTer?
ENST00000611156.4:c.433dup ENSP00000483265.1:p.Arg145ProfsTer?
NM_020469.2:c.436dup NP_065202.2:p.Arg146ProfsTer?
NM_020469.3:c.436dup NP_065202.2:p.Arg146ProfsTer?