Canonical Allele Identifier: CA1929349855
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989061G= , CM000672.2:g.94989061G= GRCh38
NC_000010.10:g.96748818G= , CM000672.1:g.96748818G= GRCh37
NC_000010.9:g.96738808G= NCBI36
NG_008385.1:g.55404G=
NG_008385.2:g.55904G=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*33G= MANE Select ENSP00000260682.6:n.*33G=
ENST00000643112.1:c.*515G= ENSP00000496202.1:n.*515G=
ENST00000260682.6:c.*33G= ENSP00000260682.6:n.*33G=
NM_000771.3:c.*33G= NP_000762.2:n.*33G=
NM_000771.4:c.*33G= MANE Select NP_000762.2:n.*33G=