Canonical Allele Identifier: CA377673937

Gene: CYP2C9

Linked Data

• dbSNP Id: rs2134349020
• MyVariant Identifiers: chr10:g.96708863A>C (hg19) ; chr10:g.94949106A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94949106A>C , CM000672.2:g.94949106A>C	GRCh38
NC_000010.10:g.96708863A>C , CM000672.1:g.96708863A>C	GRCh37
NC_000010.9:g.96698853A>C	NCBI36
NG_008385.1:g.15449A>C
NG_008385.2:g.15949A>C

Transcript Alleles

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