Canonical Allele Identifier: CA2954284210
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255994_133255998del , CM000671.2:g.133255994_133255998del GRCh38
NC_000009.11:g.136131381_136131385del , CM000671.1:g.136131381_136131385del GRCh37
NC_000009.10:g.135121202_135121206del NCBI36
NG_006669.1:g.21670_21674del
NG_006669.2:g.24218_24222del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.762_766del
ENST00000647353.1:n.54-4846_54-4842del
ENST00000679909.1:c.28+19164_28+19168del ENSP00000506089.1:n.28+19164_28+19168del
ENST00000453660.3:n.744_748del
ENST00000538324.2:c.730_734del ENSP00000483018.1:p.Thr244ArgfsTer?
ENST00000611156.4:c.730_734del ENSP00000483265.1:p.Thr244ArgfsTer?
NM_020469.2:c.733_737del NP_065202.2:p.Thr245ArgfsTer?
NM_020469.3:c.733_737del NP_065202.2:p.Thr245ArgfsTer?