Canonical Allele Identifier: CA377672693

Gene: CYP2C9

Linked Data

• MyVariant Identifiers: chr10:g.96701650T>G (hg19) ; chr10:g.94941893T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941893T>G , CM000672.2:g.94941893T>G	GRCh38
NC_000010.10:g.96701650T>G , CM000672.1:g.96701650T>G	GRCh37
NC_000010.9:g.96691640T>G	NCBI36
NG_008385.1:g.8236T>G
NG_008385.2:g.8736T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.204T>G MANE Select	ENSP00000260682.6:p.Tyr68Ter
ENST00000643112.1:c.204T>G	ENSP00000496202.1:p.Tyr68Ter
ENST00000645207.1:n.357T>G
ENST00000260682.6:c.204T>G	ENSP00000260682.6:p.Tyr68Ter
ENST00000461906.1:n.229T>G
NM_000771.3:c.204T>G	NP_000762.2:p.Tyr68Ter
NM_000771.4:c.204T>G MANE Select	NP_000762.2:p.Tyr68Ter