Canonical Allele Identifier: CA467780071
Gene: ABO HGNC NCBI

Linked Data

gnomAD v4: 9-133255328-G-T
MyVariant Identifiers: chr9:g.136130715G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255328G>T , CM000671.2:g.133255328G>T GRCh38
NC_000009.11:g.136130715G>T , CM000671.1:g.136130715G>T GRCh37
NC_000009.10:g.135120536G>T NCBI36
NG_006669.1:g.22340C>A
NG_006669.2:g.24888C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1432C>A
ENST00000647353.1:n.54-4176C>A
ENST00000679909.1:c.28+19834C>A ENSP00000506089.1:n.28+19834C>A
ENST00000453660.3:n.1414C>A
ENST00000611156.4:c.*338C>A ENSP00000483265.1:n.*338C>A
NM_020469.2:c.*338C>A NP_065202.2:n.*338C>A
NM_020469.3:c.*338C>A NP_065202.2:n.*338C>A
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