Canonical Allele Identifier: CA377672944
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2134343125
MyVariant Identifiers: chr10:g.96701774T>A (hg19) chr10:g.94942017T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942017T>A , CM000672.2:g.94942017T>A GRCh38
NC_000010.10:g.96701774T>A , CM000672.1:g.96701774T>A GRCh37
NC_000010.9:g.96691764T>A NCBI36
NG_008385.1:g.8360T>A
NG_008385.2:g.8860T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.328T>A MANE Select ENSP00000260682.6:p.Phe110Ile
ENST00000643112.1:c.328T>A ENSP00000496202.1:p.Phe110Ile
ENST00000645207.1:n.481T>A
ENST00000260682.6:c.328T>A ENSP00000260682.6:p.Phe110Ile
ENST00000461906.1:n.353T>A
ENST00000473496.1:n.99T>A
NM_000771.3:c.328T>A NP_000762.2:p.Phe110Ile
NM_000771.4:c.328T>A MANE Select NP_000762.2:p.Phe110Ile
Search 100 bp 5'
Search 100 bp 3'