Canonical Allele Identifier: CA377672953

Gene: CYP2C9

Linked Data

• MyVariant Identifiers: chr10:g.96701777G>T (hg19) ; chr10:g.94942020G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942020G>T , CM000672.2:g.94942020G>T	GRCh38
NC_000010.10:g.96701777G>T , CM000672.1:g.96701777G>T	GRCh37
NC_000010.9:g.96691767G>T	NCBI36
NG_008385.1:g.8363G>T
NG_008385.2:g.8863G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.331G>T MANE Select	ENSP00000260682.6:p.Gly111Ter
ENST00000643112.1:c.331G>T	ENSP00000496202.1:p.Gly111Ter
ENST00000645207.1:n.484G>T
ENST00000260682.6:c.331G>T	ENSP00000260682.6:p.Gly111Ter
ENST00000461906.1:n.356G>T
ENST00000473496.1:n.102G>T
NM_000771.3:c.331G>T	NP_000762.2:p.Gly111Ter
NM_000771.4:c.331G>T MANE Select	NP_000762.2:p.Gly111Ter