Canonical Allele Identifier: CA1929342555

Gene: CYP2C9

Linked Data

• dbSNP Id: rs2032235923

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981662C>T , CM000672.2:g.94981662C>T	GRCh38
NC_000010.10:g.96741419C>T , CM000672.1:g.96741419C>T	GRCh37
NC_000010.9:g.96731409C>T	NCBI36
NG_008385.1:g.48005C>T
NG_008385.2:g.48505C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.1149+292C>T MANE Select	ENSP00000260682.6:n.1149+292C>T
ENST00000643112.1:c.*158+292C>T	ENSP00000496202.1:n.*158+292C>T
ENST00000260682.6:c.1149+292C>T	ENSP00000260682.6:n.1149+292C>T
NM_000771.3:c.1149+292C>T	NP_000762.2:n.1149+292C>T
NM_000771.4:c.1149+292C>T MANE Select	NP_000762.2:n.1149+292C>T