Canonical Allele Identifier: CA931402158

Gene: CYP2C9

Linked Data

• gnomAD v3: 10-94974526-A-ATTTTTTTTT
• gnomAD v4: 10-94974526-A-ATTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94974534_94974535insTTTTTTTTT , CM000672.2:g.94974534_94974535insTTTTTTTTT	GRCh38
NC_000010.10:g.96734291_96734292insTTTTTTTTT , CM000672.1:g.96734291_96734292insTTTTTTTTT	GRCh37
NC_000010.9:g.96724281_96724282insTTTTTTTTT	NCBI36
NG_008385.1:g.40877_40878insTTTTTTTTT
NG_008385.2:g.41377_41378insTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.961+2289_961+2290insTTTTTTTTT MANE Select	ENSP00000260682.6:n.961+2289_961+2290insTTTTTTTTT
ENST00000643112.1:c.820-6649_820-6648insTTTTTTTTT	ENSP00000496202.1:n.820-6649_820-6648insTTTTTTTTT
ENST00000260682.6:c.961+2289_961+2290insTTTTTTTTT	ENSP00000260682.6:n.961+2289_961+2290insTTTTTTTTT
NM_000771.3:c.961+2289_961+2290insTTTTTTTTT	NP_000762.2:n.961+2289_961+2290insTTTTTTTTT
NM_000771.4:c.961+2289_961+2290insTTTTTTTTT MANE Select	NP_000762.2:n.961+2289_961+2290insTTTTTTTTT