Canonical Allele Identifier: CA211694063

Gene: CYP2C9

Linked Data

• dbSNP Id: rs904134157
• gnomAD v3: 10-94942718-A-G
• gnomAD v4: 10-94942718-A-G
• MyVariant Identifiers: chr10:g.96702475A>G (hg19) ; chr10:g.94942718A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942718A>G , CM000672.2:g.94942718A>G	GRCh38
NC_000010.10:g.96702475A>G , CM000672.1:g.96702475A>G	GRCh37
NC_000010.9:g.96692465A>G	NCBI36
NG_008385.1:g.9061A>G
NG_008385.2:g.9561A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.481+377A>G MANE Select	ENSP00000260682.6:n.481+377A>G
ENST00000643112.1:c.481+377A>G	ENSP00000496202.1:n.481+377A>G
ENST00000645207.1:n.634+377A>G
ENST00000260682.6:c.481+377A>G	ENSP00000260682.6:n.481+377A>G
ENST00000461906.1:n.883A>G
ENST00000473496.1:n.252+377A>G
NM_000771.3:c.481+377A>G	NP_000762.2:n.481+377A>G
NM_000771.4:c.481+377A>G MANE Select	NP_000762.2:n.481+377A>G