Canonical Allele Identifier: CA1929296154
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94947417T= , CM000672.2:g.94947417T= GRCh38
NC_000010.10:g.96707174T= , CM000672.1:g.96707174T= GRCh37
NC_000010.9:g.96697164T= NCBI36
NG_008385.1:g.13760T=
NG_008385.2:g.14260T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.482-362T= MANE Select ENSP00000260682.6:n.482-362T=
ENST00000643112.1:c.482-362T= ENSP00000496202.1:n.482-362T=
ENST00000645207.1:n.635-362T=
ENST00000260682.6:c.482-362T= ENSP00000260682.6:n.482-362T=
ENST00000473496.1:n.253-362T=
NM_000771.3:c.482-362T= NP_000762.2:n.482-362T=
NM_000771.4:c.482-362T= MANE Select NP_000762.2:n.482-362T=