Canonical Allele Identifier: CA984892851
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595033T>A , CM000679.2:g.56595033T>A GRCh38
NC_000017.10:g.54672394T>A , CM000679.1:g.54672394T>A GRCh37
NC_000017.9:g.52027393T>A NCBI36
NG_011958.1:g.6335T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*111T>A MANE Select ENSP00000328181.4:n.*111T>A
ENST00000332822.4:c.*111T>A ENSP00000328181.4:n.*111T>A
NM_005450.4:c.*111T>A NP_005441.1:n.*111T>A
NM_005450.6:c.*111T>A MANE Select NP_005441.1:n.*111T>A