Canonical Allele Identifier: CA467780811
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs557466174
gnomAD v3: 9-133255447-A-T
gnomAD v4: 9-133255447-A-T
MyVariant Identifiers: chr9:g.136130834A>T (hg19) chr9:g.133255447A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255447A>T , CM000671.2:g.133255447A>T GRCh38
NC_000009.11:g.136130834A>T , CM000671.1:g.136130834A>T GRCh37
NC_000009.10:g.135120655A>T NCBI36
NG_006669.1:g.22221T>A
NG_006669.2:g.24769T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1313T>A
ENST00000647353.1:n.54-4295T>A
ENST00000679909.1:c.28+19715T>A ENSP00000506089.1:n.28+19715T>A
ENST00000453660.3:n.1295T>A
ENST00000611156.4:c.*219T>A ENSP00000483265.1:n.*219T>A
NM_020469.2:c.*219T>A NP_065202.2:n.*219T>A
NM_020469.3:c.*219T>A NP_065202.2:n.*219T>A
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