Canonical Allele Identifier: CA377677212
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989026T>C , CM000672.2:g.94989026T>C GRCh38
NC_000010.10:g.96748783T>C , CM000672.1:g.96748783T>C GRCh37
NC_000010.9:g.96738773T>C NCBI36
NG_008385.1:g.55369T>C
NG_008385.2:g.55869T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1471T>C MANE Select ENSP00000260682.6:p.Ter491Arg
ENST00000643112.1:c.*480T>C ENSP00000496202.1:n.*480T>C
ENST00000260682.6:c.1471T>C ENSP00000260682.6:p.Ter491Arg
NM_000771.3:c.1471T>C NP_000762.2:p.Ter491Arg
NM_000771.4:c.1471T>C MANE Select NP_000762.2:p.Ter491Arg