Canonical Allele Identifier: CA2552863719
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261646del , CM000671.2:g.133261646del GRCh38
NC_000009.11:g.136137049del , CM000671.1:g.136137049del GRCh37
NC_000009.10:g.135126870del NCBI36
NG_006669.1:g.16009del
NG_006669.2:g.18574del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.129-267del
ENST00000647353.1:n.54-10489del
ENST00000651471.1:n.134-267del
ENST00000679909.1:c.28+13521del ENSP00000506089.1:n.28+13521del
ENST00000453660.3:n.111-267del
ENST00000538324.2:c.99-267del ENSP00000483018.1:n.99-267del
ENST00000611156.4:c.99-267del ENSP00000483265.1:n.99-267del
NM_020469.2:c.99-267del NP_065202.2:n.99-267del
NM_020469.3:c.99-267del NP_065202.2:n.99-267del
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