Canonical Allele Identifier: CA1929298232
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949090A= , CM000672.2:g.94949090A= GRCh38
NC_000010.10:g.96708847A= , CM000672.1:g.96708847A= GRCh37
NC_000010.9:g.96698837A= NCBI36
NG_008385.1:g.15433A=
NG_008385.2:g.15933A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-18A= MANE Select ENSP00000260682.6:n.643-18A=
ENST00000643112.1:c.643-18A= ENSP00000496202.1:n.643-18A=
ENST00000260682.6:c.643-18A= ENSP00000260682.6:n.643-18A=
ENST00000473496.1:n.414-18A=
NM_000771.3:c.643-18A= NP_000762.2:n.643-18A=
NM_000771.4:c.643-18A= MANE Select NP_000762.2:n.643-18A=