Canonical Allele Identifier: CA2610267719

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94941783-TATC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941786_94941788del , CM000672.2:g.94941786_94941788del	GRCh38
NC_000010.10:g.96701543_96701545del , CM000672.1:g.96701543_96701545del	GRCh37
NC_000010.9:g.96691533_96691535del	NCBI36
NG_008385.1:g.8129_8131del
NG_008385.2:g.8629_8631del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.169-72_169-70del MANE Select	ENSP00000260682.6:n.169-72_169-70del
ENST00000643112.1:c.169-72_169-70del	ENSP00000496202.1:n.169-72_169-70del
ENST00000645207.1:n.250_252del
ENST00000260682.6:c.169-72_169-70del	ENSP00000260682.6:n.169-72_169-70del
ENST00000461906.1:n.194-72_194-70del
NM_000771.3:c.169-72_169-70del	NP_000762.2:n.169-72_169-70del
NM_000771.4:c.169-72_169-70del MANE Select	NP_000762.2:n.169-72_169-70del