Canonical Allele Identifier: CA377672635
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96701622A>C (hg19) chr10:g.94941865A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941865A>C , CM000672.2:g.94941865A>C GRCh38
NC_000010.10:g.96701622A>C , CM000672.1:g.96701622A>C GRCh37
NC_000010.9:g.96691612A>C NCBI36
NG_008385.1:g.8208A>C
NG_008385.2:g.8708A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.176A>C MANE Select ENSP00000260682.6:p.Lys59Thr
ENST00000643112.1:c.176A>C ENSP00000496202.1:p.Lys59Thr
ENST00000645207.1:n.329A>C
ENST00000260682.6:c.176A>C ENSP00000260682.6:p.Lys59Thr
ENST00000461906.1:n.201A>C
NM_000771.3:c.176A>C NP_000762.2:p.Lys59Thr
NM_000771.4:c.176A>C MANE Select NP_000762.2:p.Lys59Thr
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