Canonical Allele Identifier: CA377672947
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96701775T>A (hg19) chr10:g.94942018T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942018T>A , CM000672.2:g.94942018T>A GRCh38
NC_000010.10:g.96701775T>A , CM000672.1:g.96701775T>A GRCh37
NC_000010.9:g.96691765T>A NCBI36
NG_008385.1:g.8361T>A
NG_008385.2:g.8861T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.329T>A MANE Select ENSP00000260682.6:p.Phe110Tyr
ENST00000643112.1:c.329T>A ENSP00000496202.1:p.Phe110Tyr
ENST00000645207.1:n.482T>A
ENST00000260682.6:c.329T>A ENSP00000260682.6:p.Phe110Tyr
ENST00000461906.1:n.354T>A
ENST00000473496.1:n.100T>A
NM_000771.3:c.329T>A NP_000762.2:p.Phe110Tyr
NM_000771.4:c.329T>A MANE Select NP_000762.2:p.Phe110Tyr
Search 100 bp 5'
Search 100 bp 3'