Canonical Allele Identifier: CA2610267680

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94941698-T-TATA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941701_94941703dup , CM000672.2:g.94941701_94941703dup	GRCh38
NC_000010.10:g.96701458_96701460dup , CM000672.1:g.96701458_96701460dup	GRCh37
NC_000010.9:g.96691448_96691450dup	NCBI36
NG_008385.1:g.8044_8046dup
NG_008385.2:g.8544_8546dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.169-157_169-155dup MANE Select	ENSP00000260682.6:n.169-157_169-155dup
ENST00000643112.1:c.169-157_169-155dup	ENSP00000496202.1:n.169-157_169-155dup
ENST00000645207.1:n.165_167dup
ENST00000260682.6:c.169-157_169-155dup	ENSP00000260682.6:n.169-157_169-155dup
ENST00000461906.1:n.194-157_194-155dup
NM_000771.3:c.169-157_169-155dup	NP_000762.2:n.169-157_169-155dup
NM_000771.4:c.169-157_169-155dup MANE Select	NP_000762.2:n.169-157_169-155dup