Canonical Allele Identifier: CA1929341988
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981239C= , CM000672.2:g.94981239C= GRCh38
NC_000010.10:g.96740996C= , CM000672.1:g.96740996C= GRCh37
NC_000010.9:g.96730986C= NCBI36
NG_008385.1:g.47582C=
NG_008385.2:g.48082C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1018C= MANE Select ENSP00000260682.6:p.Gln340=
ENST00000643112.1:c.*27C= ENSP00000496202.1:n.*27C=
ENST00000260682.6:c.1018C= ENSP00000260682.6:p.Gln340=
NM_000771.3:c.1018C= NP_000762.2:p.Gln340=
NM_000771.4:c.1018C= MANE Select NP_000762.2:p.Gln340=