Canonical Allele Identifier: CA377672899
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941994T>A , CM000672.2:g.94941994T>A GRCh38
NC_000010.10:g.96701751T>A , CM000672.1:g.96701751T>A GRCh37
NC_000010.9:g.96691741T>A NCBI36
NG_008385.1:g.8337T>A
NG_008385.2:g.8837T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.305T>A MANE Select ENSP00000260682.6:p.Leu102Gln
ENST00000643112.1:c.305T>A ENSP00000496202.1:p.Leu102Gln
ENST00000645207.1:n.458T>A
ENST00000260682.6:c.305T>A ENSP00000260682.6:p.Leu102Gln
ENST00000461906.1:n.330T>A
ENST00000473496.1:n.76T>A
NM_000771.3:c.305T>A NP_000762.2:p.Leu102Gln
NM_000771.4:c.305T>A MANE Select NP_000762.2:p.Leu102Gln