Canonical Allele Identifier: CA1929292362
Gene: CYP2C9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942157G= , CM000672.2:g.94942157G= GRCh38
NC_000010.10:g.96701914G= , CM000672.1:g.96701914G= GRCh37
NC_000010.9:g.96691904G= NCBI36
NG_008385.1:g.8500G=
NG_008385.2:g.9000G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.332-35G= MANE Select ENSP00000260682.6:n.332-35G=
ENST00000643112.1:c.332-35G= ENSP00000496202.1:n.332-35G=
ENST00000645207.1:n.485-35G=
ENST00000260682.6:c.332-35G= ENSP00000260682.6:n.332-35G=
ENST00000461906.1:n.357-35G=
ENST00000473496.1:n.103-35G=
NM_000771.3:c.332-35G= NP_000762.2:n.332-35G=
NM_000771.4:c.332-35G= MANE Select NP_000762.2:n.332-35G=
Search 100 bp 5'
Search 100 bp 3'