Canonical Allele Identifier: CA377677164
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96748760A>G (hg19) chr10:g.94989003A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989003A>G , CM000672.2:g.94989003A>G GRCh38
NC_000010.10:g.96748760A>G , CM000672.1:g.96748760A>G GRCh37
NC_000010.9:g.96738750A>G NCBI36
NG_008385.1:g.55346A>G
NG_008385.2:g.55846A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1448A>G MANE Select ENSP00000260682.6:p.Tyr483Cys
ENST00000643112.1:c.*457A>G ENSP00000496202.1:n.*457A>G
ENST00000260682.6:c.1448A>G ENSP00000260682.6:p.Tyr483Cys
NM_000771.3:c.1448A>G NP_000762.2:p.Tyr483Cys
NM_000771.4:c.1448A>G MANE Select NP_000762.2:p.Tyr483Cys
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