Canonical Allele Identifier: CA377672712
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96701658T>C (hg19) chr10:g.94941901T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941901T>C , CM000672.2:g.94941901T>C GRCh38
NC_000010.10:g.96701658T>C , CM000672.1:g.96701658T>C GRCh37
NC_000010.9:g.96691648T>C NCBI36
NG_008385.1:g.8244T>C
NG_008385.2:g.8744T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.212T>C MANE Select ENSP00000260682.6:p.Leu71Pro
ENST00000643112.1:c.212T>C ENSP00000496202.1:p.Leu71Pro
ENST00000645207.1:n.365T>C
ENST00000260682.6:c.212T>C ENSP00000260682.6:p.Leu71Pro
ENST00000461906.1:n.237T>C
NM_000771.3:c.212T>C NP_000762.2:p.Leu71Pro
NM_000771.4:c.212T>C MANE Select NP_000762.2:p.Leu71Pro
Search 100 bp 5'
Search 100 bp 3'