Canonical Allele Identifier: CA2670005152
Gene: SLC2A9 HGNC NCBI

Linked Data

gnomAD v4: 4-10034742-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.10034742G>T , CM000666.2:g.10034742G>T GRCh38
NC_000004.11:g.10036366G>T , CM000666.1:g.10036366G>T GRCh37
NC_000004.10:g.9645464G>T NCBI36
NG_011540.1:g.10507C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000309065.7:c.-41+5388C>A ENSP00000311383.3:n.-41+5388C>A
ENST00000481042.1:n.1658C>A
ENST00000505104.5:n.81+5388C>A
ENST00000506583.5:c.-41+5388C>A ENSP00000422209.1:n.-41+5388C>A
ENST00000513129.1:c.-40-8736C>A ENSP00000426800.1:n.-40-8736C>A
NM_001001290.1:c.-41+5388C>A NP_001001290.1:n.-41+5388C>A
XM_006713969.2:c.-41+5388C>A XP_006714032.1:n.-41+5388C>A
XM_011513857.1:c.-41+5388C>A XP_011512159.1:n.-41+5388C>A
NM_001001290.2:c.-41+5388C>A NP_001001290.1:n.-41+5388C>A
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