Canonical Allele Identifier: CA1929297976

Gene: CYP2C9

Linked Data

• dbSNP Id: rs779534829

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94948868G>T , CM000672.2:g.94948868G>T	GRCh38
NC_000010.10:g.96708625G>T , CM000672.1:g.96708625G>T	GRCh37
NC_000010.9:g.96698615G>T	NCBI36
NG_008385.1:g.15211G>T
NG_008385.2:g.15711G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.643-240G>T MANE Select	ENSP00000260682.6:n.643-240G>T
ENST00000643112.1:c.643-240G>T	ENSP00000496202.1:n.643-240G>T
ENST00000260682.6:c.643-240G>T	ENSP00000260682.6:n.643-240G>T
ENST00000473496.1:n.414-240G>T
NM_000771.3:c.643-240G>T	NP_000762.2:n.643-240G>T
NM_000771.4:c.643-240G>T MANE Select	NP_000762.2:n.643-240G>T