Canonical Allele Identifier: CA5616970
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs538852786

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941901T>G , CM000672.2:g.94941901T>G GRCh38
NC_000010.10:g.96701658T>G , CM000672.1:g.96701658T>G GRCh37
NC_000010.9:g.96691648T>G NCBI36
NG_008385.1:g.8244T>G
NG_008385.2:g.8744T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.212T>G MANE Select ENSP00000260682.6:p.Leu71Arg
ENST00000643112.1:c.212T>G ENSP00000496202.1:p.Leu71Arg
ENST00000645207.1:n.365T>G
ENST00000260682.6:c.212T>G ENSP00000260682.6:p.Leu71Arg
ENST00000461906.1:n.237T>G
NM_000771.3:c.212T>G NP_000762.2:p.Leu71Arg
NM_000771.4:c.212T>G MANE Select NP_000762.2:p.Leu71Arg