Canonical Allele Identifier: CA670161128

Gene: CYP2C9

Linked Data

• dbSNP Id: rs1227157186
• gnomAD v3: 10-94947128-AAACAAAAAACAACAAC-A
• gnomAD v4: 10-94947128-AAACAAAAAACAACAAC-A
• MyVariant Identifiers: chr10:g.96706886_96706901del (hg19) ; chr10:g.94947129_94947144del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94947147_94947162del , CM000672.2:g.94947147_94947162del	GRCh38
NC_000010.10:g.96706904_96706919del , CM000672.1:g.96706904_96706919del	GRCh37
NC_000010.9:g.96696894_96696909del	NCBI36
NG_008385.1:g.13490_13505del
NG_008385.2:g.13990_14005del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.482-632_482-617del MANE Select	ENSP00000260682.6:n.482-632_482-617del
ENST00000643112.1:c.482-632_482-617del	ENSP00000496202.1:n.482-632_482-617del
ENST00000645207.1:n.635-632_635-617del
ENST00000260682.6:c.482-632_482-617del	ENSP00000260682.6:n.482-632_482-617del
ENST00000473496.1:n.253-632_253-617del
NM_000771.3:c.482-632_482-617del	NP_000762.2:n.482-632_482-617del
NM_000771.4:c.482-632_482-617del MANE Select	NP_000762.2:n.482-632_482-617del