Canonical Allele Identifier: CA1929292670
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942728T= , CM000672.2:g.94942728T= GRCh38
NC_000010.10:g.96702485T= , CM000672.1:g.96702485T= GRCh37
NC_000010.9:g.96692475T= NCBI36
NG_008385.1:g.9071T=
NG_008385.2:g.9571T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+387T= MANE Select ENSP00000260682.6:n.481+387T=
ENST00000643112.1:c.481+387T= ENSP00000496202.1:n.481+387T=
ENST00000645207.1:n.634+387T=
ENST00000260682.6:c.481+387T= ENSP00000260682.6:n.481+387T=
ENST00000461906.1:n.893T=
ENST00000473496.1:n.252+387T=
NM_000771.3:c.481+387T= NP_000762.2:n.481+387T=
NM_000771.4:c.481+387T= MANE Select NP_000762.2:n.481+387T=
Search 100 bp 5'
Search 100 bp 3'