Canonical Allele Identifier: CA1929297904
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94948799T= , CM000672.2:g.94948799T= GRCh38
NC_000010.10:g.96708556T= , CM000672.1:g.96708556T= GRCh37
NC_000010.9:g.96698546T= NCBI36
NG_008385.1:g.15142T=
NG_008385.2:g.15642T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-309T= MANE Select ENSP00000260682.6:n.643-309T=
ENST00000643112.1:c.643-309T= ENSP00000496202.1:n.643-309T=
ENST00000260682.6:c.643-309T= ENSP00000260682.6:n.643-309T=
ENST00000473496.1:n.414-309T=
NM_000771.3:c.643-309T= NP_000762.2:n.643-309T=
NM_000771.4:c.643-309T= MANE Select NP_000762.2:n.643-309T=