Canonical Allele Identifier: CA670159196

Gene: CYP2C9

Linked Data

• dbSNP Id: rs1271867785
• gnomAD v3: 10-94942524-A-G
• gnomAD v4: 10-94942524-A-G
• MyVariant Identifiers: chr10:g.96702281A>G (hg19) ; chr10:g.94942524A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942524A>G , CM000672.2:g.94942524A>G	GRCh38
NC_000010.10:g.96702281A>G , CM000672.1:g.96702281A>G	GRCh37
NC_000010.9:g.96692271A>G	NCBI36
NG_008385.1:g.8867A>G
NG_008385.2:g.9367A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.481+183A>G MANE Select	ENSP00000260682.6:n.481+183A>G
ENST00000643112.1:c.481+183A>G	ENSP00000496202.1:n.481+183A>G
ENST00000645207.1:n.634+183A>G
ENST00000260682.6:c.481+183A>G	ENSP00000260682.6:n.481+183A>G
ENST00000461906.1:n.689A>G
ENST00000473496.1:n.252+183A>G
NM_000771.3:c.481+183A>G	NP_000762.2:n.481+183A>G
NM_000771.4:c.481+183A>G MANE Select	NP_000762.2:n.481+183A>G