Canonical Allele Identifier: CA2610268084

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94942692-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942692C>T , CM000672.2:g.94942692C>T	GRCh38
NC_000010.10:g.96702449C>T , CM000672.1:g.96702449C>T	GRCh37
NC_000010.9:g.96692439C>T	NCBI36
NG_008385.1:g.9035C>T
NG_008385.2:g.9535C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.481+351C>T MANE Select	ENSP00000260682.6:n.481+351C>T
ENST00000643112.1:c.481+351C>T	ENSP00000496202.1:n.481+351C>T
ENST00000645207.1:n.634+351C>T
ENST00000260682.6:c.481+351C>T	ENSP00000260682.6:n.481+351C>T
ENST00000461906.1:n.857C>T
ENST00000473496.1:n.252+351C>T
NM_000771.3:c.481+351C>T	NP_000762.2:n.481+351C>T
NM_000771.4:c.481+351C>T MANE Select	NP_000762.2:n.481+351C>T