Canonical Allele Identifier: CA377677155
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96748757T>A (hg19) chr10:g.94989000T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989000T>A , CM000672.2:g.94989000T>A GRCh38
NC_000010.10:g.96748757T>A , CM000672.1:g.96748757T>A GRCh37
NC_000010.9:g.96738747T>A NCBI36
NG_008385.1:g.55343T>A
NG_008385.2:g.55843T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1445T>A MANE Select ENSP00000260682.6:p.Phe482Tyr
ENST00000643112.1:c.*454T>A ENSP00000496202.1:n.*454T>A
ENST00000260682.6:c.1445T>A ENSP00000260682.6:p.Phe482Tyr
NM_000771.3:c.1445T>A NP_000762.2:p.Phe482Tyr
NM_000771.4:c.1445T>A MANE Select NP_000762.2:p.Phe482Tyr
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