Canonical Allele Identifier: CA377677032
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988939G>C , CM000672.2:g.94988939G>C GRCh38
NC_000010.10:g.96748696G>C , CM000672.1:g.96748696G>C GRCh37
NC_000010.9:g.96738686G>C NCBI36
NG_008385.1:g.55282G>C
NG_008385.2:g.55782G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1384G>C MANE Select ENSP00000260682.6:p.Val462Leu
ENST00000643112.1:c.*393G>C ENSP00000496202.1:n.*393G>C
ENST00000260682.6:c.1384G>C ENSP00000260682.6:p.Val462Leu
NM_000771.3:c.1384G>C NP_000762.2:p.Val462Leu
NM_000771.4:c.1384G>C MANE Select NP_000762.2:p.Val462Leu