Canonical Allele Identifier: CA399964830
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594434G>A , CM000679.2:g.56594434G>A GRCh38
NC_000017.10:g.54671795G>A , CM000679.1:g.54671795G>A GRCh37
NC_000017.9:g.52026794G>A NCBI36
NG_011958.1:g.5736G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.211G>A MANE Select ENSP00000328181.4:p.Gly71Arg
ENST00000332822.4:c.211G>A ENSP00000328181.4:p.Gly71Arg
NM_005450.4:c.211G>A NP_005441.1:p.Gly71Arg
NM_005450.6:c.211G>A MANE Select NP_005441.1:p.Gly71Arg