Canonical Allele Identifier: CA5617016
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs374133592
ExAC: 10:96701910 C / G
gnomAD v2: 10-96701910-C-G
gnomAD v3: 10-94942153-C-G
gnomAD v4: 10-94942153-C-G
MyVariant Identifiers: chr10:g.96701910C>G (hg19) chr10:g.94942153C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942153C>G , CM000672.2:g.94942153C>G GRCh38
NC_000010.10:g.96701910C>G , CM000672.1:g.96701910C>G GRCh37
NC_000010.9:g.96691900C>G NCBI36
NG_008385.1:g.8496C>G
NG_008385.2:g.8996C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.332-39C>G MANE Select ENSP00000260682.6:n.332-39C>G
ENST00000643112.1:c.332-39C>G ENSP00000496202.1:n.332-39C>G
ENST00000645207.1:n.485-39C>G
ENST00000260682.6:c.332-39C>G ENSP00000260682.6:n.332-39C>G
ENST00000461906.1:n.357-39C>G
ENST00000473496.1:n.103-39C>G
NM_000771.3:c.332-39C>G NP_000762.2:n.332-39C>G
NM_000771.4:c.332-39C>G MANE Select NP_000762.2:n.332-39C>G
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