Canonical Allele Identifier: CA377676899
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96748630C>G (hg19) chr10:g.94988873C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988873C>G , CM000672.2:g.94988873C>G GRCh38
NC_000010.10:g.96748630C>G , CM000672.1:g.96748630C>G GRCh37
NC_000010.9:g.96738620C>G NCBI36
NG_008385.1:g.55216C>G
NG_008385.2:g.55716C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1318C>G MANE Select ENSP00000260682.6:p.Leu440Val
ENST00000643112.1:c.*327C>G ENSP00000496202.1:n.*327C>G
ENST00000260682.6:c.1318C>G ENSP00000260682.6:p.Leu440Val
NM_000771.3:c.1318C>G NP_000762.2:p.Leu440Val
NM_000771.4:c.1318C>G MANE Select NP_000762.2:p.Leu440Val
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