Canonical Allele Identifier: CA200766502
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs514708
gnomAD v3: 9-133258352-C-T
gnomAD v4: 9-133258352-C-T
MyVariant Identifiers: chr9:g.133258352C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258352C>T , CM000671.2:g.133258352C>T GRCh38
NG_006669.1:g.19311G>A
NG_006669.2:g.21863G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-220G>A
ENST00000647353.1:n.54-7200G>A
ENST00000651471.1:n.239-220G>A
ENST00000679909.1:c.28+16810G>A ENSP00000506089.1:n.28+16810G>A
ENST00000453660.3:n.216-220G>A
ENST00000538324.2:c.204-220G>A ENSP00000483018.1:n.204-220G>A
ENST00000611156.4:c.204-220G>A ENSP00000483265.1:n.204-220G>A
NM_020469.2:c.204-220G>A NP_065202.2:n.204-220G>A
NM_020469.3:c.204-220G>A NP_065202.2:n.204-220G>A
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