Canonical Allele Identifier: CA5616955

Gene: CYP2C9

Linked Data

• dbSNP Id: rs756921618
• ExAC: 10:96701590 CTGT / C
• gnomAD v2: 10-96701590-CTGT-C
• gnomAD v4: 10-94941833-CTGT-C
• MyVariant Identifiers: chr10:g.96701591_96701593del (hg19) ; chr10:g.94941834_94941836del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941835_94941837del , CM000672.2:g.94941835_94941837del	GRCh38
NC_000010.10:g.96701592_96701594del , CM000672.1:g.96701592_96701594del	GRCh37
NC_000010.9:g.96691582_96691584del	NCBI36
NG_008385.1:g.8178_8180del
NG_008385.2:g.8678_8680del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.169-23_169-21del MANE Select	ENSP00000260682.6:n.169-23_169-21del
ENST00000643112.1:c.169-23_169-21del	ENSP00000496202.1:n.169-23_169-21del
ENST00000645207.1:n.299_301del
ENST00000260682.6:c.169-23_169-21del	ENSP00000260682.6:n.169-23_169-21del
ENST00000461906.1:n.194-23_194-21del
NM_000771.3:c.169-23_169-21del	NP_000762.2:n.169-23_169-21del
NM_000771.4:c.169-23_169-21del MANE Select	NP_000762.2:n.169-23_169-21del