Canonical Allele Identifier: CA377672633
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2031390725
gnomAD v3: 10-94941864-A-G
gnomAD v4: 10-94941864-A-G
MyVariant Identifiers: chr10:g.96701621A>G (hg19) chr10:g.94941864A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941864A>G , CM000672.2:g.94941864A>G GRCh38
NC_000010.10:g.96701621A>G , CM000672.1:g.96701621A>G GRCh37
NC_000010.9:g.96691611A>G NCBI36
NG_008385.1:g.8207A>G
NG_008385.2:g.8707A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.175A>G MANE Select ENSP00000260682.6:p.Lys59Glu
ENST00000643112.1:c.175A>G ENSP00000496202.1:p.Lys59Glu
ENST00000645207.1:n.328A>G
ENST00000260682.6:c.175A>G ENSP00000260682.6:p.Lys59Glu
ENST00000461906.1:n.200A>G
NM_000771.3:c.175A>G NP_000762.2:p.Lys59Glu
NM_000771.4:c.175A>G MANE Select NP_000762.2:p.Lys59Glu
Search 100 bp 5'
Search 100 bp 3'