Canonical Allele Identifier: CA1929292376

Gene: CYP2C9

Linked Data

• dbSNP Id: rs2031399651

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942178dup , CM000672.2:g.94942178dup	GRCh38
NC_000010.10:g.96701935dup , CM000672.1:g.96701935dup	GRCh37
NC_000010.9:g.96691925dup	NCBI36
NG_008385.1:g.8521dup
NG_008385.2:g.9021dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.332-14dup MANE Select	ENSP00000260682.6:n.332-14dup
ENST00000643112.1:c.332-14dup	ENSP00000496202.1:n.332-14dup
ENST00000645207.1:n.485-14dup
ENST00000260682.6:c.332-14dup	ENSP00000260682.6:n.332-14dup
ENST00000461906.1:n.357-14dup
ENST00000473496.1:n.103-14dup
NM_000771.3:c.332-14dup	NP_000762.2:n.332-14dup
NM_000771.4:c.332-14dup MANE Select	NP_000762.2:n.332-14dup