Canonical Allele Identifier: CA1437812242
Gene: SLC2A9 HGNC NCBI

Linked Data

dbSNP Id: rs948897569
gnomAD v3: 4-10034902-G-C
gnomAD v4: 4-10034902-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.10034902G>C , CM000666.2:g.10034902G>C GRCh38
NC_000004.11:g.10036526G>C , CM000666.1:g.10036526G>C GRCh37
NC_000004.10:g.9645624G>C NCBI36
NG_011540.1:g.10347C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309065.7:c.-41+5228C>G ENSP00000311383.3:n.-41+5228C>G
ENST00000481042.1:n.1498C>G
ENST00000505104.5:n.81+5228C>G
ENST00000506583.5:c.-41+5228C>G ENSP00000422209.1:n.-41+5228C>G
ENST00000513129.1:c.-40-8896C>G ENSP00000426800.1:n.-40-8896C>G
NM_001001290.1:c.-41+5228C>G NP_001001290.1:n.-41+5228C>G
XM_006713969.2:c.-41+5228C>G XP_006714032.1:n.-41+5228C>G
XM_011513857.1:c.-41+5228C>G XP_011512159.1:n.-41+5228C>G
NM_001001290.2:c.-41+5228C>G NP_001001290.1:n.-41+5228C>G