Canonical Allele Identifier: CA377672671
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96701639T>G (hg19) chr10:g.94941882T>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.193T>G MANE Select ENSP00000260682.6:p.Phe65Val
ENST00000643112.1:c.193T>G ENSP00000496202.1:p.Phe65Val
ENST00000645207.1:n.346T>G
ENST00000260682.6:c.193T>G ENSP00000260682.6:p.Phe65Val
ENST00000461906.1:n.218T>G
NM_000771.3:c.193T>G NP_000762.2:p.Phe65Val
NM_000771.4:c.193T>G MANE Select NP_000762.2:p.Phe65Val
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