Canonical Allele Identifier: CA470837451
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2032368306
gnomAD v3: 10-94989008-C-T
gnomAD v4: 10-94989008-C-T
MyVariant Identifiers: chr10:g.96748765C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989008C>T , CM000672.2:g.94989008C>T GRCh38
NC_000010.10:g.96748765C>T , CM000672.1:g.96748765C>T GRCh37
NC_000010.9:g.96738755C>T NCBI36
NG_008385.1:g.55351C>T
NG_008385.2:g.55851C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1453C>T MANE Select ENSP00000260682.6:p.Leu485=
ENST00000643112.1:c.*462C>T ENSP00000496202.1:n.*462C>T
ENST00000260682.6:c.1453C>T ENSP00000260682.6:p.Leu485=
NM_000771.3:c.1453C>T NP_000762.2:p.Leu485=
NM_000771.4:c.1453C>T MANE Select NP_000762.2:p.Leu485=
Search 100 bp 5'
Search 100 bp 3'