Canonical Allele Identifier: CA1929297911
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94948804A= , CM000672.2:g.94948804A= GRCh38
NC_000010.10:g.96708561A= , CM000672.1:g.96708561A= GRCh37
NC_000010.9:g.96698551A= NCBI36
NG_008385.1:g.15147A=
NG_008385.2:g.15647A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-304A= MANE Select ENSP00000260682.6:n.643-304A=
ENST00000643112.1:c.643-304A= ENSP00000496202.1:n.643-304A=
ENST00000260682.6:c.643-304A= ENSP00000260682.6:n.643-304A=
ENST00000473496.1:n.414-304A=
NM_000771.3:c.643-304A= NP_000762.2:n.643-304A=
NM_000771.4:c.643-304A= MANE Select NP_000762.2:n.643-304A=