Canonical Allele Identifier: CA670178459

Gene: CYP2C9

Linked Data

• dbSNP Id: rs1554866849
• gnomAD v3: 10-94974531-T-TTTTG
• gnomAD v4: 10-94974531-T-TTTTG
• MyVariant Identifiers: chr10:g.96734288_96734289insTTTG (hg19) ; chr10:g.94974531_94974532insTTTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94974535_94974538dup , CM000672.2:g.94974535_94974538dup	GRCh38
NC_000010.10:g.96734292_96734295dup , CM000672.1:g.96734292_96734295dup	GRCh37
NC_000010.9:g.96724282_96724285dup	NCBI36
NG_008385.1:g.40878_40881dup
NG_008385.2:g.41378_41381dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.961+2290_961+2293dup MANE Select	ENSP00000260682.6:n.961+2290_961+2293dup
ENST00000643112.1:c.820-6648_820-6645dup	ENSP00000496202.1:n.820-6648_820-6645dup
ENST00000260682.6:c.961+2290_961+2293dup	ENSP00000260682.6:n.961+2290_961+2293dup
NM_000771.3:c.961+2290_961+2293dup	NP_000762.2:n.961+2290_961+2293dup
NM_000771.4:c.961+2290_961+2293dup MANE Select	NP_000762.2:n.961+2290_961+2293dup