Canonical Allele Identifier: CA467780182
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs878903450
gnomAD v3: 9-133255359-A-T
gnomAD v4: 9-133255359-A-T
MyVariant Identifiers: chr9:g.136130746A>T (hg19) chr9:g.133255359A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255359A>T , CM000671.2:g.133255359A>T GRCh38
NC_000009.11:g.136130746A>T , CM000671.1:g.136130746A>T GRCh37
NC_000009.10:g.135120567A>T NCBI36
NG_006669.1:g.22309T>A
NG_006669.2:g.24857T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1401T>A
ENST00000647353.1:n.54-4207T>A
ENST00000679909.1:c.28+19803T>A ENSP00000506089.1:n.28+19803T>A
ENST00000453660.3:n.1383T>A
ENST00000611156.4:c.*307T>A ENSP00000483265.1:n.*307T>A
NM_020469.2:c.*307T>A NP_065202.2:n.*307T>A
NM_020469.3:c.*307T>A NP_065202.2:n.*307T>A
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