Canonical Allele Identifier: CA377676183
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981214T>G , CM000672.2:g.94981214T>G GRCh38
NC_000010.10:g.96740971T>G , CM000672.1:g.96740971T>G GRCh37
NC_000010.9:g.96730961T>G NCBI36
NG_008385.1:g.47557T>G
NG_008385.2:g.48057T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.993T>G MANE Select ENSP00000260682.6:p.Ile331Met
ENST00000643112.1:c.*2T>G ENSP00000496202.1:n.*2T>G
ENST00000260682.6:c.993T>G ENSP00000260682.6:p.Ile331Met
NM_000771.3:c.993T>G NP_000762.2:p.Ile331Met
NM_000771.4:c.993T>G MANE Select NP_000762.2:p.Ile331Met