Canonical Allele Identifier: CA211692950
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs370315268

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941892A>G , CM000672.2:g.94941892A>G GRCh38
NC_000010.10:g.96701649A>G , CM000672.1:g.96701649A>G GRCh37
NC_000010.9:g.96691639A>G NCBI36
NG_008385.1:g.8235A>G
NG_008385.2:g.8735A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.203A>G MANE Select ENSP00000260682.6:p.Tyr68Cys
ENST00000643112.1:c.203A>G ENSP00000496202.1:p.Tyr68Cys
ENST00000645207.1:n.356A>G
ENST00000260682.6:c.203A>G ENSP00000260682.6:p.Tyr68Cys
ENST00000461906.1:n.228A>G
NM_000771.3:c.203A>G NP_000762.2:p.Tyr68Cys
NM_000771.4:c.203A>G MANE Select NP_000762.2:p.Tyr68Cys