Canonical Allele Identifier: CA2789072650
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942411del , CM000672.2:g.94942411del GRCh38
NC_000010.10:g.96702168del , CM000672.1:g.96702168del GRCh37
NC_000010.9:g.96692158del NCBI36
NG_008385.1:g.8754del
NG_008385.2:g.9254del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+70del MANE Select ENSP00000260682.6:n.481+70del
ENST00000643112.1:c.481+70del ENSP00000496202.1:n.481+70del
ENST00000645207.1:n.634+70del
ENST00000260682.6:c.481+70del ENSP00000260682.6:n.481+70del
ENST00000461906.1:n.576del
ENST00000473496.1:n.252+70del
NM_000771.3:c.481+70del NP_000762.2:n.481+70del
NM_000771.4:c.481+70del MANE Select NP_000762.2:n.481+70del