Canonical Allele Identifier: CA211735769

Gene: CYP2C9

Linked Data

• dbSNP Id: rs9332240
• gnomAD v2: 10-96748852-C-T
• gnomAD v3: 10-94989095-C-T
• gnomAD v4: 10-94989095-C-T
• MyVariant Identifiers: chr10:g.96748852C>T (hg19) ; chr10:g.94989095C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94989095C>T , CM000672.2:g.94989095C>T	GRCh38
NC_000010.10:g.96748852C>T , CM000672.1:g.96748852C>T	GRCh37
NC_000010.9:g.96738842C>T	NCBI36
NG_008385.1:g.55438C>T
NG_008385.2:g.55938C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.*67C>T MANE Select	ENSP00000260682.6:n.*67C>T
ENST00000643112.1:c.*549C>T	ENSP00000496202.1:n.*549C>T
ENST00000260682.6:c.*67C>T	ENSP00000260682.6:n.*67C>T
NM_000771.3:c.*67C>T	NP_000762.2:n.*67C>T
NM_000771.4:c.*67C>T MANE Select	NP_000762.2:n.*67C>T