Canonical Allele Identifier: CA1929292334
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2031398111

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942113C>A , CM000672.2:g.94942113C>A GRCh38
NC_000010.10:g.96701870C>A , CM000672.1:g.96701870C>A GRCh37
NC_000010.9:g.96691860C>A NCBI36
NG_008385.1:g.8456C>A
NG_008385.2:g.8956C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.332-79C>A MANE Select ENSP00000260682.6:n.332-79C>A
ENST00000643112.1:c.332-79C>A ENSP00000496202.1:n.332-79C>A
ENST00000645207.1:n.485-79C>A
ENST00000260682.6:c.332-79C>A ENSP00000260682.6:n.332-79C>A
ENST00000461906.1:n.357-79C>A
ENST00000473496.1:n.103-79C>A
NM_000771.3:c.332-79C>A NP_000762.2:n.332-79C>A
NM_000771.4:c.332-79C>A MANE Select NP_000762.2:n.332-79C>A