Canonical Allele Identifier: CA2692330344
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255731_133255733del , CM000671.2:g.133255731_133255733del GRCh38
NC_000009.11:g.136131118_136131120del , CM000671.1:g.136131118_136131120del GRCh37
NC_000009.10:g.135120939_135120941del NCBI36
NG_006669.1:g.21938_21940del
NG_006669.2:g.24486_24488del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1030_1032del
ENST00000647353.1:n.54-4578_54-4576del
ENST00000679909.1:c.28+19432_28+19434del ENSP00000506089.1:n.28+19432_28+19434del
ENST00000453660.3:n.1012_1014del
ENST00000538324.2:c.998_1000del ENSP00000483018.1:p.Ala333del
ENST00000611156.4:c.998_1000del ENSP00000483265.1:p.Ala333del
NM_020469.2:c.1001_1003del NP_065202.2:p.Ala334del
NM_020469.3:c.1001_1003del NP_065202.2:p.Ala334del