Canonical Allele Identifier: CA470837399
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1351633002

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988932A>G , CM000672.2:g.94988932A>G GRCh38
NC_000010.10:g.96748689A>G , CM000672.1:g.96748689A>G GRCh37
NC_000010.9:g.96738679A>G NCBI36
NG_008385.1:g.55275A>G
NG_008385.2:g.55775A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1377A>G MANE Select ENSP00000260682.6:p.Lys459=
ENST00000643112.1:c.*386A>G ENSP00000496202.1:n.*386A>G
ENST00000260682.6:c.1377A>G ENSP00000260682.6:p.Lys459=
NM_000771.3:c.1377A>G NP_000762.2:p.Lys459=
NM_000771.4:c.1377A>G MANE Select NP_000762.2:p.Lys459=