Canonical Allele Identifier: CA211692939
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs867193471

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941874G>A , CM000672.2:g.94941874G>A GRCh38
NC_000010.10:g.96701631G>A , CM000672.1:g.96701631G>A GRCh37
NC_000010.9:g.96691621G>A NCBI36
NG_008385.1:g.8217G>A
NG_008385.2:g.8717G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.185G>A MANE Select ENSP00000260682.6:p.Gly62Asp
ENST00000643112.1:c.185G>A ENSP00000496202.1:p.Gly62Asp
ENST00000645207.1:n.338G>A
ENST00000260682.6:c.185G>A ENSP00000260682.6:p.Gly62Asp
ENST00000461906.1:n.210G>A
NM_000771.3:c.185G>A NP_000762.2:p.Gly62Asp
NM_000771.4:c.185G>A MANE Select NP_000762.2:p.Gly62Asp