Canonical Allele Identifier: CA1929341784
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981138_94981139delinsGC , CM000672.2:g.94981138_94981139delinsGC GRCh38
NC_000010.10:g.96740895_96740896delinsGC , CM000672.1:g.96740895_96740896delinsGC GRCh37
NC_000010.9:g.96730885_96730886delinsGC NCBI36
NG_008385.1:g.47481_47482delinsGC
NG_008385.2:g.47981_47982delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.962-45_962-44delinsGC MANE Select ENSP00000260682.6:n.962-45_962-44delinsGC...
ENST00000643112.1:c.820-45_820-44delinsGC ENSP00000496202.1:n.820-45_820-44delinsGC...
ENST00000260682.6:c.962-45_962-44delinsGC ENSP00000260682.6:n.962-45_962-44delinsGC...
NM_000771.3:c.962-45_962-44delinsGC NP_000762.2:n.962-45_962-44delinsGC
NM_000771.4:c.962-45_962-44delinsGC MANE Select NP_000762.2:n.962-45_962-44delinsGC
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