Canonical Allele Identifier: CA1929292324

Gene: CYP2C9

Linked Data

• dbSNP Id: rs2031397864

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942101_94942102insCA , CM000672.2:g.94942101_94942102insCA	GRCh38
NC_000010.10:g.96701858_96701859insCA , CM000672.1:g.96701858_96701859insCA	GRCh37
NC_000010.9:g.96691848_96691849insCA	NCBI36
NG_008385.1:g.8444_8445insCA
NG_008385.2:g.8944_8945insCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.331+81_331+82insCA MANE Select	ENSP00000260682.6:n.331+81_331+82insCA
ENST00000643112.1:c.331+81_331+82insCA	ENSP00000496202.1:n.331+81_331+82insCA
ENST00000645207.1:n.484+81_484+82insCA
ENST00000260682.6:c.331+81_331+82insCA	ENSP00000260682.6:n.331+81_331+82insCA
ENST00000461906.1:n.356+81_356+82insCA
ENST00000473496.1:n.102+81_102+82insCA
NM_000771.3:c.331+81_331+82insCA	NP_000762.2:n.331+81_331+82insCA
NM_000771.4:c.331+81_331+82insCA MANE Select	NP_000762.2:n.331+81_331+82insCA