Canonical Allele Identifier: CA467852820
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136131389del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256003del , CM000671.2:g.133256003del GRCh38
NC_000009.11:g.136131390del , CM000671.1:g.136131390del GRCh37
NC_000009.10:g.135121211del NCBI36
NG_006669.1:g.21666del
NG_006669.2:g.24214del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.758del
ENST00000647353.1:n.54-4850del
ENST00000679909.1:c.28+19160del ENSP00000506089.1:n.28+19160del
ENST00000453660.3:n.740del
ENST00000538324.2:c.726del ENSP00000483018.1:p.Phe243SerfsTer?
ENST00000611156.4:c.726del ENSP00000483265.1:p.Phe243SerfsTer?
NM_020469.2:c.729del NP_065202.2:p.Phe244SerfsTer?
NM_020469.3:c.729del NP_065202.2:p.Phe244SerfsTer?