Canonical Allele Identifier: CA1929349501
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988862T= , CM000672.2:g.94988862T= GRCh38
NC_000010.10:g.96748619T= , CM000672.1:g.96748619T= GRCh37
NC_000010.9:g.96738609T= NCBI36
NG_008385.1:g.55205T=
NG_008385.2:g.55705T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1307T= MANE Select ENSP00000260682.6:p.Val436=
ENST00000643112.1:c.*316T= ENSP00000496202.1:n.*316T=
ENST00000260682.6:c.1307T= ENSP00000260682.6:p.Val436=
NM_000771.3:c.1307T= NP_000762.2:p.Val436=
NM_000771.4:c.1307T= MANE Select NP_000762.2:p.Val436=
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