Canonical Allele Identifier: CA595638787

Gene: CYP2C9

Linked Data

• dbSNP Id: rs1325659431
• gnomAD v2: 10-96707415-CTT-C
• MyVariant Identifiers: chr10:g.96707416_96707417del (hg19) ; chr10:g.94947659_94947660del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94947663_94947664del , CM000672.2:g.94947663_94947664del	GRCh38
NC_000010.10:g.96707420_96707421del , CM000672.1:g.96707420_96707421del	GRCh37
NC_000010.9:g.96697410_96697411del	NCBI36
NG_008385.1:g.14006_14007del
NG_008385.2:g.14506_14507del

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.482-116_482-115del MANE Select	ENSP00000260682.6:n.482-116_482-115del
ENST00000643112.1:c.482-116_482-115del	ENSP00000496202.1:n.482-116_482-115del
ENST00000645207.1:n.635-116_635-115del
ENST00000260682.6:c.482-116_482-115del	ENSP00000260682.6:n.482-116_482-115del
ENST00000473496.1:n.253-116_253-115del
NM_000771.3:c.482-116_482-115del	NP_000762.2:n.482-116_482-115del
NM_000771.4:c.482-116_482-115del MANE Select	NP_000762.2:n.482-116_482-115del