Canonical Allele Identifier: CA2266876291
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594618G= , CM000679.2:g.56594618G= GRCh38
NC_000017.10:g.54671979G= , CM000679.1:g.54671979G= GRCh37
NC_000017.9:g.52026978G= NCBI36
NG_011958.1:g.5920G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.395G= MANE Select ENSP00000328181.4:p.Gly132=
ENST00000332822.4:c.395G= ENSP00000328181.4:p.Gly132=
NM_005450.4:c.395G= NP_005441.1:p.Gly132=
NM_005450.6:c.395G= MANE Select NP_005441.1:p.Gly132=