Canonical Allele Identifier: CA1437815511
Gene: SLC2A9 HGNC NCBI

Linked Data

dbSNP Id: rs13137343

Genomic Alleles

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

Transcript Alleles

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