Canonical Allele Identifier: CA377672803
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941944A>C , CM000672.2:g.94941944A>C GRCh38
NC_000010.10:g.96701701A>C , CM000672.1:g.96701701A>C GRCh37
NC_000010.9:g.96691691A>C NCBI36
NG_008385.1:g.8287A>C
NG_008385.2:g.8787A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.255A>C MANE Select ENSP00000260682.6:p.Glu85Asp
ENST00000643112.1:c.255A>C ENSP00000496202.1:p.Glu85Asp
ENST00000645207.1:n.408A>C
ENST00000260682.6:c.255A>C ENSP00000260682.6:p.Glu85Asp
ENST00000461906.1:n.280A>C
ENST00000473496.1:n.26A>C
NM_000771.3:c.255A>C NP_000762.2:p.Glu85Asp
NM_000771.4:c.255A>C MANE Select NP_000762.2:p.Glu85Asp