Canonical Allele Identifier: CA377676950
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96748656C>A (hg19) chr10:g.94988899C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988899C>A , CM000672.2:g.94988899C>A GRCh38
NC_000010.10:g.96748656C>A , CM000672.1:g.96748656C>A GRCh37
NC_000010.9:g.96738646C>A NCBI36
NG_008385.1:g.55242C>A
NG_008385.2:g.55742C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1344C>A MANE Select ENSP00000260682.6:p.Phe448Leu
ENST00000643112.1:c.*353C>A ENSP00000496202.1:n.*353C>A
ENST00000260682.6:c.1344C>A ENSP00000260682.6:p.Phe448Leu
NM_000771.3:c.1344C>A NP_000762.2:p.Phe448Leu
NM_000771.4:c.1344C>A MANE Select NP_000762.2:p.Phe448Leu
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