Canonical Allele Identifier: CA377676939
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96748651T>G (hg19) chr10:g.94988894T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988894T>G , CM000672.2:g.94988894T>G GRCh38
NC_000010.10:g.96748651T>G , CM000672.1:g.96748651T>G GRCh37
NC_000010.9:g.96738641T>G NCBI36
NG_008385.1:g.55237T>G
NG_008385.2:g.55737T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1339T>G MANE Select ENSP00000260682.6:p.Leu447Val
ENST00000643112.1:c.*348T>G ENSP00000496202.1:n.*348T>G
ENST00000260682.6:c.1339T>G ENSP00000260682.6:p.Leu447Val
NM_000771.3:c.1339T>G NP_000762.2:p.Leu447Val
NM_000771.4:c.1339T>G MANE Select NP_000762.2:p.Leu447Val
Search 100 bp 5'
Search 100 bp 3'