Canonical Allele Identifier: CA470837394
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96748680T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988923T>C , CM000672.2:g.94988923T>C GRCh38
NC_000010.10:g.96748680T>C , CM000672.1:g.96748680T>C GRCh37
NC_000010.9:g.96738670T>C NCBI36
NG_008385.1:g.55266T>C
NG_008385.2:g.55766T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1368T>C MANE Select ENSP00000260682.6:p.Phe456=
ENST00000643112.1:c.*377T>C ENSP00000496202.1:n.*377T>C
ENST00000260682.6:c.1368T>C ENSP00000260682.6:p.Phe456=
NM_000771.3:c.1368T>C NP_000762.2:p.Phe456=
NM_000771.4:c.1368T>C MANE Select NP_000762.2:p.Phe456=