Canonical Allele Identifier: CA2610267783

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94942145-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942145T>G , CM000672.2:g.94942145T>G	GRCh38
NC_000010.10:g.96701902T>G , CM000672.1:g.96701902T>G	GRCh37
NC_000010.9:g.96691892T>G	NCBI36
NG_008385.1:g.8488T>G
NG_008385.2:g.8988T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.332-47T>G MANE Select	ENSP00000260682.6:n.332-47T>G
ENST00000643112.1:c.332-47T>G	ENSP00000496202.1:n.332-47T>G
ENST00000645207.1:n.485-47T>G
ENST00000260682.6:c.332-47T>G	ENSP00000260682.6:n.332-47T>G
ENST00000461906.1:n.357-47T>G
ENST00000473496.1:n.103-47T>G
NM_000771.3:c.332-47T>G	NP_000762.2:n.332-47T>G
NM_000771.4:c.332-47T>G MANE Select	NP_000762.2:n.332-47T>G