Canonical Allele Identifier: CA1929296292

Gene: CYP2C9

Linked Data

• dbSNP Id: rs2031518414

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94947567del , CM000672.2:g.94947567del	GRCh38
NC_000010.10:g.96707324del , CM000672.1:g.96707324del	GRCh37
NC_000010.9:g.96697314del	NCBI36
NG_008385.1:g.13910del
NG_008385.2:g.14410del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.482-212del MANE Select	ENSP00000260682.6:n.482-212del
ENST00000643112.1:c.482-212del	ENSP00000496202.1:n.482-212del
ENST00000645207.1:n.635-212del
ENST00000260682.6:c.482-212del	ENSP00000260682.6:n.482-212del
ENST00000473496.1:n.253-212del
NM_000771.3:c.482-212del	NP_000762.2:n.482-212del
NM_000771.4:c.482-212del MANE Select	NP_000762.2:n.482-212del