Canonical Allele Identifier: CA470837368
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96748638C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988881C>A , CM000672.2:g.94988881C>A GRCh38
NC_000010.10:g.96748638C>A , CM000672.1:g.96748638C>A GRCh37
NC_000010.9:g.96738628C>A NCBI36
NG_008385.1:g.55224C>A
NG_008385.2:g.55724C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1326C>A MANE Select ENSP00000260682.6:p.Gly442=
ENST00000643112.1:c.*335C>A ENSP00000496202.1:n.*335C>A
ENST00000260682.6:c.1326C>A ENSP00000260682.6:p.Gly442=
NM_000771.3:c.1326C>A NP_000762.2:p.Gly442=
NM_000771.4:c.1326C>A MANE Select NP_000762.2:p.Gly442=
Search 100 bp 5'
Search 100 bp 3'