Canonical Allele Identifier: CA1929296262

Gene: CYP2C9

Linked Data

• dbSNP Id: rs2031517800

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94947531A>T , CM000672.2:g.94947531A>T	GRCh38
NC_000010.10:g.96707288A>T , CM000672.1:g.96707288A>T	GRCh37
NC_000010.9:g.96697278A>T	NCBI36
NG_008385.1:g.13874A>T
NG_008385.2:g.14374A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.482-248A>T MANE Select	ENSP00000260682.6:n.482-248A>T
ENST00000643112.1:c.482-248A>T	ENSP00000496202.1:n.482-248A>T
ENST00000645207.1:n.635-248A>T
ENST00000260682.6:c.482-248A>T	ENSP00000260682.6:n.482-248A>T
ENST00000473496.1:n.253-248A>T
NM_000771.3:c.482-248A>T	NP_000762.2:n.482-248A>T
NM_000771.4:c.482-248A>T MANE Select	NP_000762.2:n.482-248A>T