Canonical Allele Identifier: CA1929349868
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989080C= , CM000672.2:g.94989080C= GRCh38
NC_000010.10:g.96748837C= , CM000672.1:g.96748837C= GRCh37
NC_000010.9:g.96738827C= NCBI36
NG_008385.1:g.55423C=
NG_008385.2:g.55923C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*52C= MANE Select ENSP00000260682.6:n.*52C=
ENST00000643112.1:c.*534C= ENSP00000496202.1:n.*534C=
ENST00000260682.6:c.*52C= ENSP00000260682.6:n.*52C=
NM_000771.3:c.*52C= NP_000762.2:n.*52C=
NM_000771.4:c.*52C= MANE Select NP_000762.2:n.*52C=