Canonical Allele Identifier: CA211700261

Gene: CYP2C9

Linked Data

• dbSNP Id: rs560483134
• gnomAD v2: 10-96708835-T-G
• gnomAD v3: 10-94949078-T-G
• gnomAD v4: 10-94949078-T-G
• MyVariant Identifiers: chr10:g.96708835T>G (hg19) ; chr10:g.94949078T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94949078T>G , CM000672.2:g.94949078T>G	GRCh38
NC_000010.10:g.96708835T>G , CM000672.1:g.96708835T>G	GRCh37
NC_000010.9:g.96698825T>G	NCBI36
NG_008385.1:g.15421T>G
NG_008385.2:g.15921T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.643-30T>G MANE Select	ENSP00000260682.6:n.643-30T>G
ENST00000643112.1:c.643-30T>G	ENSP00000496202.1:n.643-30T>G
ENST00000260682.6:c.643-30T>G	ENSP00000260682.6:n.643-30T>G
ENST00000473496.1:n.414-30T>G
NM_000771.3:c.643-30T>G	NP_000762.2:n.643-30T>G
NM_000771.4:c.643-30T>G MANE Select	NP_000762.2:n.643-30T>G