Canonical Allele Identifier: CA92230370
Gene: SLC2A9 HGNC NCBI

Linked Data

dbSNP Id: rs896673383
MyVariant Identifiers: chr4:g.10036565A>G (hg19) chr4:g.10034941A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.10034941A>G , CM000666.2:g.10034941A>G GRCh38
NC_000004.11:g.10036565A>G , CM000666.1:g.10036565A>G GRCh37
NC_000004.10:g.9645663A>G NCBI36
NG_011540.1:g.10308T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309065.7:c.-41+5189T>C ENSP00000311383.3:n.-41+5189T>C
ENST00000481042.1:n.1459T>C
ENST00000505104.5:n.81+5189T>C
ENST00000506583.5:c.-41+5189T>C ENSP00000422209.1:n.-41+5189T>C
ENST00000513129.1:c.-40-8935T>C ENSP00000426800.1:n.-40-8935T>C
NM_001001290.1:c.-41+5189T>C NP_001001290.1:n.-41+5189T>C
XM_006713969.2:c.-41+5189T>C XP_006714032.1:n.-41+5189T>C
XM_011513857.1:c.-41+5189T>C XP_011512159.1:n.-41+5189T>C
NM_001001290.2:c.-41+5189T>C NP_001001290.1:n.-41+5189T>C
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