Canonical Allele Identifier: CA591309062
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1182603501
gnomAD v2: 9-136132959-TG-T
MyVariant Identifiers: chr9:g.136132960del (hg19) chr9:g.133257573del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257574del , CM000671.2:g.133257574del GRCh38
NC_000009.11:g.136132961del , CM000671.1:g.136132961del GRCh37
NC_000009.10:g.135122782del NCBI36
NG_006669.1:g.20094del
NG_006669.2:g.22642del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-31del
ENST00000647353.1:n.54-6421del
ENST00000651471.1:n.329+469del
ENST00000679909.1:c.28+17589del ENSP00000506089.1:n.28+17589del
ENST00000453660.3:n.252-31del
ENST00000538324.2:c.240-31del ENSP00000483018.1:n.240-31del
ENST00000611156.4:c.240-31del ENSP00000483265.1:n.240-31del
NM_020469.2:c.240-31del NP_065202.2:n.240-31del
NM_020469.3:c.240-31del NP_065202.2:n.240-31del
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