Canonical Allele Identifier: CA211698489

Gene: CYP2C9

Linked Data

• dbSNP Id: rs113926940
• gnomAD v2: 10-96707186-C-A
• gnomAD v3: 10-94947429-C-A
• gnomAD v4: 10-94947429-C-A
• MyVariant Identifiers: chr10:g.96707186C>A (hg19) ; chr10:g.94947429C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94947429C>A , CM000672.2:g.94947429C>A	GRCh38
NC_000010.10:g.96707186C>A , CM000672.1:g.96707186C>A	GRCh37
NC_000010.9:g.96697176C>A	NCBI36
NG_008385.1:g.13772C>A
NG_008385.2:g.14272C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.482-350C>A MANE Select	ENSP00000260682.6:n.482-350C>A
ENST00000643112.1:c.482-350C>A	ENSP00000496202.1:n.482-350C>A
ENST00000645207.1:n.635-350C>A
ENST00000260682.6:c.482-350C>A	ENSP00000260682.6:n.482-350C>A
ENST00000473496.1:n.253-350C>A
NM_000771.3:c.482-350C>A	NP_000762.2:n.482-350C>A
NM_000771.4:c.482-350C>A MANE Select	NP_000762.2:n.482-350C>A