Canonical Allele Identifier: CA1929349876
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989098C= , CM000672.2:g.94989098C= GRCh38
NC_000010.10:g.96748855C= , CM000672.1:g.96748855C= GRCh37
NC_000010.9:g.96738845C= NCBI36
NG_008385.1:g.55441C=
NG_008385.2:g.55941C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*70C= MANE Select ENSP00000260682.6:n.*70C=
ENST00000643112.1:c.*552C= ENSP00000496202.1:n.*552C=
ENST00000260682.6:c.*70C= ENSP00000260682.6:n.*70C=
NM_000771.3:c.*70C= NP_000762.2:n.*70C=
NM_000771.4:c.*70C= MANE Select NP_000762.2:n.*70C=