Canonical Allele Identifier: CA984892991
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595104A>T , CM000679.2:g.56595104A>T GRCh38
NC_000017.10:g.54672465A>T , CM000679.1:g.54672465A>T GRCh37
NC_000017.9:g.52027464A>T NCBI36
NG_011958.1:g.6406A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*182A>T MANE Select ENSP00000328181.4:n.*182A>T
ENST00000332822.4:c.*182A>T ENSP00000328181.4:n.*182A>T
NM_005450.4:c.*182A>T NP_005441.1:n.*182A>T
NM_005450.6:c.*182A>T MANE Select NP_005441.1:n.*182A>T