Canonical Allele Identifier: CA784341336
Gene: SLC2A9 HGNC NCBI

Linked Data

dbSNP Id: rs1421341613
MyVariant Identifiers: chr4:g.10036642G>T (hg19) chr4:g.10035018G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.10035018G>T , CM000666.2:g.10035018G>T GRCh38
NC_000004.11:g.10036642G>T , CM000666.1:g.10036642G>T GRCh37
NC_000004.10:g.9645740G>T NCBI36
NG_011540.1:g.10231C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309065.7:c.-41+5112C>A ENSP00000311383.3:n.-41+5112C>A
ENST00000481042.1:n.1382C>A
ENST00000505104.5:n.81+5112C>A
ENST00000506583.5:c.-41+5112C>A ENSP00000422209.1:n.-41+5112C>A
ENST00000513129.1:c.-40-9012C>A ENSP00000426800.1:n.-40-9012C>A
NM_001001290.1:c.-41+5112C>A NP_001001290.1:n.-41+5112C>A
XM_006713969.2:c.-41+5112C>A XP_006714032.1:n.-41+5112C>A
XM_011513857.1:c.-41+5112C>A XP_011512159.1:n.-41+5112C>A
NM_001001290.2:c.-41+5112C>A NP_001001290.1:n.-41+5112C>A
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