Canonical Allele Identifier: CA1929298176
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949041G= , CM000672.2:g.94949041G= GRCh38
NC_000010.10:g.96708798G= , CM000672.1:g.96708798G= GRCh37
NC_000010.9:g.96698788G= NCBI36
NG_008385.1:g.15384G=
NG_008385.2:g.15884G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-67G= MANE Select ENSP00000260682.6:n.643-67G=
ENST00000643112.1:c.643-67G= ENSP00000496202.1:n.643-67G=
ENST00000260682.6:c.643-67G= ENSP00000260682.6:n.643-67G=
ENST00000473496.1:n.414-67G=
NM_000771.3:c.643-67G= NP_000762.2:n.643-67G=
NM_000771.4:c.643-67G= MANE Select NP_000762.2:n.643-67G=
Search 100 bp 5'
Search 100 bp 3'