Canonical Allele Identifier: CA5617299
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs56165452

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981297T>C , CM000672.2:g.94981297T>C GRCh38
NC_000010.10:g.96741054T>C , CM000672.1:g.96741054T>C GRCh37
NC_000010.9:g.96731044T>C NCBI36
NG_008385.1:g.47640T>C
NG_008385.2:g.48140T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1076T>C MANE Select ENSP00000260682.6:p.Ile359Thr
ENST00000643112.1:c.*85T>C ENSP00000496202.1:n.*85T>C
ENST00000260682.6:c.1076T>C ENSP00000260682.6:p.Ile359Thr
NM_000771.3:c.1076T>C NP_000762.2:p.Ile359Thr
NM_000771.4:c.1076T>C MANE Select NP_000762.2:p.Ile359Thr