Canonical Allele Identifier: CA211735534
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs200382419

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988889T>A , CM000672.2:g.94988889T>A GRCh38
NC_000010.10:g.96748646T>A , CM000672.1:g.96748646T>A GRCh37
NC_000010.9:g.96738636T>A NCBI36
NG_008385.1:g.55232T>A
NG_008385.2:g.55732T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1334T>A MANE Select ENSP00000260682.6:p.Leu445Gln
ENST00000643112.1:c.*343T>A ENSP00000496202.1:n.*343T>A
ENST00000260682.6:c.1334T>A ENSP00000260682.6:p.Leu445Gln
NM_000771.3:c.1334T>A NP_000762.2:p.Leu445Gln
NM_000771.4:c.1334T>A MANE Select NP_000762.2:p.Leu445Gln