Canonical Allele Identifier: CA2610267784

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94942154-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942154T>G , CM000672.2:g.94942154T>G	GRCh38
NC_000010.10:g.96701911T>G , CM000672.1:g.96701911T>G	GRCh37
NC_000010.9:g.96691901T>G	NCBI36
NG_008385.1:g.8497T>G
NG_008385.2:g.8997T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.332-38T>G MANE Select	ENSP00000260682.6:n.332-38T>G
ENST00000643112.1:c.332-38T>G	ENSP00000496202.1:n.332-38T>G
ENST00000645207.1:n.485-38T>G
ENST00000260682.6:c.332-38T>G	ENSP00000260682.6:n.332-38T>G
ENST00000461906.1:n.357-38T>G
ENST00000473496.1:n.103-38T>G
NM_000771.3:c.332-38T>G	NP_000762.2:n.332-38T>G
NM_000771.4:c.332-38T>G MANE Select	NP_000762.2:n.332-38T>G