Canonical Allele Identifier: CA377677099
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96748727T>A (hg19) chr10:g.94988970T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988970T>A , CM000672.2:g.94988970T>A GRCh38
NC_000010.10:g.96748727T>A , CM000672.1:g.96748727T>A GRCh37
NC_000010.9:g.96738717T>A NCBI36
NG_008385.1:g.55313T>A
NG_008385.2:g.55813T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1415T>A MANE Select ENSP00000260682.6:p.Val472Asp
ENST00000643112.1:c.*424T>A ENSP00000496202.1:n.*424T>A
ENST00000260682.6:c.1415T>A ENSP00000260682.6:p.Val472Asp
NM_000771.3:c.1415T>A NP_000762.2:p.Val472Asp
NM_000771.4:c.1415T>A MANE Select NP_000762.2:p.Val472Asp
Search 100 bp 5'
Search 100 bp 3'