Canonical Allele Identifier: CA1929292269
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942034T= , CM000672.2:g.94942034T= GRCh38
NC_000010.10:g.96701791T= , CM000672.1:g.96701791T= GRCh37
NC_000010.9:g.96691781T= NCBI36
NG_008385.1:g.8377T=
NG_008385.2:g.8877T=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.331+14T= MANE Select ENSP00000260682.6:n.331+14T=
ENST00000643112.1:c.331+14T= ENSP00000496202.1:n.331+14T=
ENST00000645207.1:n.484+14T=
ENST00000260682.6:c.331+14T= ENSP00000260682.6:n.331+14T=
ENST00000461906.1:n.356+14T=
ENST00000473496.1:n.102+14T=
NM_000771.3:c.331+14T= NP_000762.2:n.331+14T=
NM_000771.4:c.331+14T= MANE Select NP_000762.2:n.331+14T=
Search 100 bp 5'
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