Canonical Allele Identifier: CA1929292156
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941828G= , CM000672.2:g.94941828G= GRCh38
NC_000010.10:g.96701585G= , CM000672.1:g.96701585G= GRCh37
NC_000010.9:g.96691575G= NCBI36
NG_008385.1:g.8171G=
NG_008385.2:g.8671G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.169-30G= MANE Select ENSP00000260682.6:n.169-30G=
ENST00000643112.1:c.169-30G= ENSP00000496202.1:n.169-30G=
ENST00000645207.1:n.292G=
ENST00000260682.6:c.169-30G= ENSP00000260682.6:n.169-30G=
ENST00000461906.1:n.194-30G=
NM_000771.3:c.169-30G= NP_000762.2:n.169-30G=
NM_000771.4:c.169-30G= MANE Select NP_000762.2:n.169-30G=
Search 100 bp 5'
Search 100 bp 3'