Canonical Allele Identifier: CA1929292165
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941843T= , CM000672.2:g.94941843T= GRCh38
NC_000010.10:g.96701600T= , CM000672.1:g.96701600T= GRCh37
NC_000010.9:g.96691590T= NCBI36
NG_008385.1:g.8186T=
NG_008385.2:g.8686T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.169-15T= MANE Select ENSP00000260682.6:n.169-15T=
ENST00000643112.1:c.169-15T= ENSP00000496202.1:n.169-15T=
ENST00000645207.1:n.307T=
ENST00000260682.6:c.169-15T= ENSP00000260682.6:n.169-15T=
ENST00000461906.1:n.194-15T=
NM_000771.3:c.169-15T= NP_000762.2:n.169-15T=
NM_000771.4:c.169-15T= MANE Select NP_000762.2:n.169-15T=
Search 100 bp 5'
Search 100 bp 3'