Canonical Allele Identifier: CA377677178
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989009T>C , CM000672.2:g.94989009T>C GRCh38
NC_000010.10:g.96748766T>C , CM000672.1:g.96748766T>C GRCh37
NC_000010.9:g.96738756T>C NCBI36
NG_008385.1:g.55352T>C
NG_008385.2:g.55852T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1454T>C MANE Select ENSP00000260682.6:p.Leu485Pro
ENST00000643112.1:c.*463T>C ENSP00000496202.1:n.*463T>C
ENST00000260682.6:c.1454T>C ENSP00000260682.6:p.Leu485Pro
NM_000771.3:c.1454T>C NP_000762.2:p.Leu485Pro
NM_000771.4:c.1454T>C MANE Select NP_000762.2:p.Leu485Pro