Canonical Allele Identifier: CA119590
Gene: CYP2C9 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 8408
dbSNP Id: rs1057910

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981296A>C , CM000672.2:g.94981296A>C GRCh38
NC_000010.10:g.96741053A>C , CM000672.1:g.96741053A>C GRCh37
NC_000010.9:g.96731043A>C NCBI36
NG_008385.1:g.47639A>C
NG_008385.2:g.48139A>C

Transcript Alleles

HGVS Amino-acid change
NM_000771.3:c.1075A>C VV NP_000762.2:p.Ile359Leu
NM_000771.4:c.1075A>C VV NP_000762.2:p.Ile359Leu
ENST00000260682.6:c.1075A>C ENSP00000260682.6:p.Ile359Leu