Canonical Allele Identifier: CA670178458

Gene: CYP2C9

Linked Data

• dbSNP Id: rs1554866848
• MyVariant Identifiers: chr10:g.96734288_96734289insTTTTG (hg19) ; chr10:g.94974531_94974532insTTTTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94974534_94974535insTGTTT , CM000672.2:g.94974534_94974535insTGTTT	GRCh38
NC_000010.10:g.96734291_96734292insTGTTT , CM000672.1:g.96734291_96734292insTGTTT	GRCh37
NC_000010.9:g.96724281_96724282insTGTTT	NCBI36
NG_008385.1:g.40877_40878insTGTTT
NG_008385.2:g.41377_41378insTGTTT

Transcript Alleles

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