Canonical Allele Identifier: CA595638803

Gene: CYP2C9

Linked Data

• dbSNP Id: rs1193579305
• gnomAD v2: 10-96701794-C-G
• gnomAD v4: 10-94942037-C-G
• MyVariant Identifiers: chr10:g.96701794C>G (hg19) ; chr10:g.94942037C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942037C>G , CM000672.2:g.94942037C>G	GRCh38
NC_000010.10:g.96701794C>G , CM000672.1:g.96701794C>G	GRCh37
NC_000010.9:g.96691784C>G	NCBI36
NG_008385.1:g.8380C>G
NG_008385.2:g.8880C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.331+17C>G MANE Select	ENSP00000260682.6:n.331+17C>G
ENST00000643112.1:c.331+17C>G	ENSP00000496202.1:n.331+17C>G
ENST00000645207.1:n.484+17C>G
ENST00000260682.6:c.331+17C>G	ENSP00000260682.6:n.331+17C>G
ENST00000461906.1:n.356+17C>G
ENST00000473496.1:n.102+17C>G
NM_000771.3:c.331+17C>G	NP_000762.2:n.331+17C>G
NM_000771.4:c.331+17C>G MANE Select	NP_000762.2:n.331+17C>G