Canonical Allele Identifier: CA2266876398
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594914T= , CM000679.2:g.56594914T= GRCh38
NC_000017.10:g.54672275T= , CM000679.1:g.54672275T= GRCh37
NC_000017.9:g.52027274T= NCBI36
NG_011958.1:g.6216T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.691T= MANE Select ENSP00000328181.4:p.Ser231=
ENST00000332822.4:c.691T= ENSP00000328181.4:p.Ser231=
NM_005450.4:c.691T= NP_005441.1:p.Ser231=
NM_005450.6:c.691T= MANE Select NP_005441.1:p.Ser231=