Canonical Allele Identifier: CA1929349892
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989126C= , CM000672.2:g.94989126C= GRCh38
NC_000010.10:g.96748883C= , CM000672.1:g.96748883C= GRCh37
NC_000010.9:g.96738873C= NCBI36
NG_008385.1:g.55469C=
NG_008385.2:g.55969C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.*98C= MANE Select ENSP00000260682.6:n.*98C=
ENST00000643112.1:c.*580C= ENSP00000496202.1:n.*580C=
ENST00000260682.6:c.*98C= ENSP00000260682.6:n.*98C=
NM_000771.3:c.*98C= NP_000762.2:n.*98C=
NM_000771.4:c.*98C= MANE Select NP_000762.2:n.*98C=