Canonical Allele Identifier: CA2266876536
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595100G= , CM000679.2:g.56595100G= GRCh38
NC_000017.10:g.54672461G= , CM000679.1:g.54672461G= GRCh37
NC_000017.9:g.52027460G= NCBI36
NG_011958.1:g.6402G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*178G= MANE Select ENSP00000328181.4:n.*178G=
ENST00000332822.4:c.*178G= ENSP00000328181.4:n.*178G=
NM_005450.4:c.*178G= NP_005441.1:n.*178G=
NM_005450.6:c.*178G= MANE Select NP_005441.1:n.*178G=