Canonical Allele Identifier: CA377677213
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989026T>G , CM000672.2:g.94989026T>G GRCh38
NC_000010.10:g.96748783T>G , CM000672.1:g.96748783T>G GRCh37
NC_000010.9:g.96738773T>G NCBI36
NG_008385.1:g.55369T>G
NG_008385.2:g.55869T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1471T>G MANE Select ENSP00000260682.6:p.Ter491Gly
ENST00000643112.1:c.*480T>G ENSP00000496202.1:n.*480T>G
ENST00000260682.6:c.1471T>G ENSP00000260682.6:p.Ter491Gly
NM_000771.3:c.1471T>G NP_000762.2:p.Ter491Gly
NM_000771.4:c.1471T>G MANE Select NP_000762.2:p.Ter491Gly