Canonical Allele Identifier: CA377672634

Gene: CYP2C9

Linked Data

• dbSNP Id: rs2031390725
• MyVariant Identifiers: chr10:g.96701621A>T (hg19) ; chr10:g.94941864A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941864A>T , CM000672.2:g.94941864A>T	GRCh38
NC_000010.10:g.96701621A>T , CM000672.1:g.96701621A>T	GRCh37
NC_000010.9:g.96691611A>T	NCBI36
NG_008385.1:g.8207A>T
NG_008385.2:g.8707A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.175A>T MANE Select	ENSP00000260682.6:p.Lys59Ter
ENST00000643112.1:c.175A>T	ENSP00000496202.1:p.Lys59Ter
ENST00000645207.1:n.328A>T
ENST00000260682.6:c.175A>T	ENSP00000260682.6:p.Lys59Ter
ENST00000461906.1:n.200A>T
NM_000771.3:c.175A>T	NP_000762.2:p.Lys59Ter
NM_000771.4:c.175A>T MANE Select	NP_000762.2:p.Lys59Ter