Canonical Allele Identifier: CA918736890

Gene: CYP2C9

Linked Data

• dbSNP Id: rs1589404965
• gnomAD v4: 10-94941788-TGCTAAATCAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941792_94941801del , CM000672.2:g.94941792_94941801del	GRCh38
NC_000010.10:g.96701549_96701558del , CM000672.1:g.96701549_96701558del	GRCh37
NC_000010.9:g.96691539_96691548del	NCBI36
NG_008385.1:g.8135_8144del
NG_008385.2:g.8635_8644del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.169-66_169-57del MANE Select	ENSP00000260682.6:n.169-66_169-57del
ENST00000643112.1:c.169-66_169-57del	ENSP00000496202.1:n.169-66_169-57del
ENST00000645207.1:n.256_265del
ENST00000260682.6:c.169-66_169-57del	ENSP00000260682.6:n.169-66_169-57del
ENST00000461906.1:n.194-66_194-57del
NM_000771.3:c.169-66_169-57del	NP_000762.2:n.169-66_169-57del
NM_000771.4:c.169-66_169-57del MANE Select	NP_000762.2:n.169-66_169-57del