Canonical Allele Identifier: CA377672670
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1176755716
gnomAD v2: 10-96701639-T-C
gnomAD v4: 10-94941882-T-C
MyVariant Identifiers: chr10:g.96701639T>C (hg19) chr10:g.94941882T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941882T>C , CM000672.2:g.94941882T>C GRCh38
NC_000010.10:g.96701639T>C , CM000672.1:g.96701639T>C GRCh37
NC_000010.9:g.96691629T>C NCBI36
NG_008385.1:g.8225T>C
NG_008385.2:g.8725T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.193T>C MANE Select ENSP00000260682.6:p.Phe65Leu
ENST00000643112.1:c.193T>C ENSP00000496202.1:p.Phe65Leu
ENST00000645207.1:n.346T>C
ENST00000260682.6:c.193T>C ENSP00000260682.6:p.Phe65Leu
ENST00000461906.1:n.218T>C
NM_000771.3:c.193T>C NP_000762.2:p.Phe65Leu
NM_000771.4:c.193T>C MANE Select NP_000762.2:p.Phe65Leu
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