Canonical Allele Identifier: CA377677208
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989023G>C , CM000672.2:g.94989023G>C GRCh38
NC_000010.10:g.96748780G>C , CM000672.1:g.96748780G>C GRCh37
NC_000010.9:g.96738770G>C NCBI36
NG_008385.1:g.55366G>C
NG_008385.2:g.55866G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1468G>C MANE Select ENSP00000260682.6:p.Val490Leu
ENST00000643112.1:c.*477G>C ENSP00000496202.1:n.*477G>C
ENST00000260682.6:c.1468G>C ENSP00000260682.6:p.Val490Leu
NM_000771.3:c.1468G>C NP_000762.2:p.Val490Leu
NM_000771.4:c.1468G>C MANE Select NP_000762.2:p.Val490Leu