Canonical Allele Identifier: CA2266876386
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594871C= , CM000679.2:g.56594871C= GRCh38
NC_000017.10:g.54672232C= , CM000679.1:g.54672232C= GRCh37
NC_000017.9:g.52027231C= NCBI36
NG_011958.1:g.6173C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.648C= MANE Select ENSP00000328181.4:p.Gly216=
ENST00000332822.4:c.648C= ENSP00000328181.4:p.Gly216=
NM_005450.4:c.648C= NP_005441.1:p.Gly216=
NM_005450.6:c.648C= MANE Select NP_005441.1:p.Gly216=