Canonical Allele Identifier: CA1929349822
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988992G= , CM000672.2:g.94988992G= GRCh38
NC_000010.10:g.96748749G= , CM000672.1:g.96748749G= GRCh37
NC_000010.9:g.96738739G= NCBI36
NG_008385.1:g.55335G=
NG_008385.2:g.55835G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1437G= MANE Select ENSP00000260682.6:p.Val479=
ENST00000643112.1:c.*446G= ENSP00000496202.1:n.*446G=
ENST00000260682.6:c.1437G= ENSP00000260682.6:p.Val479=
NM_000771.3:c.1437G= NP_000762.2:p.Val479=
NM_000771.4:c.1437G= MANE Select NP_000762.2:p.Val479=
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