Canonical Allele Identifier: CA1929292358
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942149T= , CM000672.2:g.94942149T= GRCh38
NC_000010.10:g.96701906T= , CM000672.1:g.96701906T= GRCh37
NC_000010.9:g.96691896T= NCBI36
NG_008385.1:g.8492T=
NG_008385.2:g.8992T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.332-43T= MANE Select ENSP00000260682.6:n.332-43T=
ENST00000643112.1:c.332-43T= ENSP00000496202.1:n.332-43T=
ENST00000645207.1:n.485-43T=
ENST00000260682.6:c.332-43T= ENSP00000260682.6:n.332-43T=
ENST00000461906.1:n.357-43T=
ENST00000473496.1:n.103-43T=
NM_000771.3:c.332-43T= NP_000762.2:n.332-43T=
NM_000771.4:c.332-43T= MANE Select NP_000762.2:n.332-43T=
Search 100 bp 5'
Search 100 bp 3'