Canonical Allele Identifier: CA377677218
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989028A>G , CM000672.2:g.94989028A>G GRCh38
NC_000010.10:g.96748785A>G , CM000672.1:g.96748785A>G GRCh37
NC_000010.9:g.96738775A>G NCBI36
NG_008385.1:g.55371A>G
NG_008385.2:g.55871A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1473A>G MANE Select ENSP00000260682.6:p.Ter491Trp
ENST00000643112.1:c.*482A>G ENSP00000496202.1:n.*482A>G
ENST00000260682.6:c.1473A>G ENSP00000260682.6:p.Ter491Trp
NM_000771.3:c.1473A>G NP_000762.2:p.Ter491Trp
NM_000771.4:c.1473A>G MANE Select NP_000762.2:p.Ter491Trp