Canonical Allele Identifier: CA5617431

Gene: CYP2C9

Linked Data

• dbSNP Id: rs776357745
• ExAC: 10:96748816 C / T
• gnomAD v2: 10-96748816-C-T
• gnomAD v3: 10-94989059-C-T
• gnomAD v4: 10-94989059-C-T
• MyVariant Identifiers: chr10:g.96748816C>T (hg19) ; chr10:g.94989059C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94989059C>T , CM000672.2:g.94989059C>T	GRCh38
NC_000010.10:g.96748816C>T , CM000672.1:g.96748816C>T	GRCh37
NC_000010.9:g.96738806C>T	NCBI36
NG_008385.1:g.55402C>T
NG_008385.2:g.55902C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.*31C>T MANE Select	ENSP00000260682.6:n.*31C>T
ENST00000643112.1:c.*513C>T	ENSP00000496202.1:n.*513C>T
ENST00000260682.6:c.*31C>T	ENSP00000260682.6:n.*31C>T
NM_000771.3:c.*31C>T	NP_000762.2:n.*31C>T
NM_000771.4:c.*31C>T MANE Select	NP_000762.2:n.*31C>T