Canonical Allele Identifier: CA5617407
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs759392078

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988954C>T , CM000672.2:g.94988954C>T GRCh38
NC_000010.10:g.96748711C>T , CM000672.1:g.96748711C>T GRCh37
NC_000010.9:g.96738701C>T NCBI36
NG_008385.1:g.55297C>T
NG_008385.2:g.55797C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1399C>T MANE Select ENSP00000260682.6:p.Leu467Phe
ENST00000643112.1:c.*408C>T ENSP00000496202.1:n.*408C>T
ENST00000260682.6:c.1399C>T ENSP00000260682.6:p.Leu467Phe
NM_000771.3:c.1399C>T NP_000762.2:p.Leu467Phe
NM_000771.4:c.1399C>T MANE Select NP_000762.2:p.Leu467Phe