Canonical Allele Identifier: CA1437815512
Gene: SLC2A9 HGNC NCBI

Linked Data

dbSNP Id: rs13137343
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.10041404C>T , CM000666.2:g.10041404C>T GRCh38
NC_000004.11:g.10043028C>T , CM000666.1:g.10043028C>T GRCh37
NC_000004.10:g.9652126C>T NCBI36
NG_011540.1:g.3845G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000506583.5:c.-175-1140G>A ENSP00000422209.1:n.-175-1140G>A
ENST00000513129.1:c.-41+13429G>A ENSP00000426800.1:n.-41+13429G>A
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