Canonical Allele Identifier: CA211735497
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs894084285

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988857T>G , CM000672.2:g.94988857T>G GRCh38
NC_000010.10:g.96748614T>G , CM000672.1:g.96748614T>G GRCh37
NC_000010.9:g.96738604T>G NCBI36
NG_008385.1:g.55200T>G
NG_008385.2:g.55700T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1302T>G MANE Select ENSP00000260682.6:p.Ile434Met
ENST00000643112.1:c.*311T>G ENSP00000496202.1:n.*311T>G
ENST00000260682.6:c.1302T>G ENSP00000260682.6:p.Ile434Met
NM_000771.3:c.1302T>G NP_000762.2:p.Ile434Met
NM_000771.4:c.1302T>G MANE Select NP_000762.2:p.Ile434Met