Canonical Allele Identifier: CA595321719

Gene: CYP2C9

Linked Data

• dbSNP Id: rs1476851716
• gnomAD v2: 10-96734288-T-TTTG
• gnomAD v3: 10-94974531-T-TTTG
• gnomAD v4: 10-94974531-T-TTTG
• MyVariant Identifiers: chr10:g.96734288_96734289insTTG (hg19) ; chr10:g.94974531_94974532insTTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94974533_94974534insGTT , CM000672.2:g.94974533_94974534insGTT	GRCh38
NC_000010.10:g.96734290_96734291insGTT , CM000672.1:g.96734290_96734291insGTT	GRCh37
NC_000010.9:g.96724280_96724281insGTT	NCBI36
NG_008385.1:g.40876_40877insGTT
NG_008385.2:g.41376_41377insGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.961+2288_961+2289insGTT MANE Select	ENSP00000260682.6:n.961+2288_961+2289insGTT
ENST00000643112.1:c.820-6650_820-6649insGTT	ENSP00000496202.1:n.820-6650_820-6649insGTT
ENST00000260682.6:c.961+2288_961+2289insGTT	ENSP00000260682.6:n.961+2288_961+2289insGTT
NM_000771.3:c.961+2288_961+2289insGTT	NP_000762.2:n.961+2288_961+2289insGTT
NM_000771.4:c.961+2288_961+2289insGTT MANE Select	NP_000762.2:n.961+2288_961+2289insGTT