Canonical Allele Identifier: CA211692925
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1045243646

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941862C>T , CM000672.2:g.94941862C>T GRCh38
NC_000010.10:g.96701619C>T , CM000672.1:g.96701619C>T GRCh37
NC_000010.9:g.96691609C>T NCBI36
NG_008385.1:g.8205C>T
NG_008385.2:g.8705C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.173C>T MANE Select ENSP00000260682.6:p.Ser58Leu
ENST00000643112.1:c.173C>T ENSP00000496202.1:p.Ser58Leu
ENST00000645207.1:n.326C>T
ENST00000260682.6:c.173C>T ENSP00000260682.6:p.Ser58Leu
ENST00000461906.1:n.198C>T
NM_000771.3:c.173C>T NP_000762.2:p.Ser58Leu
NM_000771.4:c.173C>T MANE Select NP_000762.2:p.Ser58Leu