Canonical Allele Identifier: CA670236184

Gene: CYP2C9

Linked Data

• dbSNP Id: rs1246677156
• MyVariant Identifiers: chr10:g.96701787C>T (hg19) ; chr10:g.94942030C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942030C>T , CM000672.2:g.94942030C>T	GRCh38
NC_000010.10:g.96701787C>T , CM000672.1:g.96701787C>T	GRCh37
NC_000010.9:g.96691777C>T	NCBI36
NG_008385.1:g.8373C>T
NG_008385.2:g.8873C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.331+10C>T MANE Select	ENSP00000260682.6:n.331+10C>T
ENST00000643112.1:c.331+10C>T	ENSP00000496202.1:n.331+10C>T
ENST00000645207.1:n.484+10C>T
ENST00000260682.6:c.331+10C>T	ENSP00000260682.6:n.331+10C>T
ENST00000461906.1:n.356+10C>T
ENST00000473496.1:n.102+10C>T
NM_000771.3:c.331+10C>T	NP_000762.2:n.331+10C>T
NM_000771.4:c.331+10C>T MANE Select	NP_000762.2:n.331+10C>T