Canonical Allele Identifier: CA2733892518
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs2145567771

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595027dup , CM000679.2:g.56595027dup GRCh38
NC_000017.10:g.54672388dup , CM000679.1:g.54672388dup GRCh37
NC_000017.9:g.52027387dup NCBI36
NG_011958.1:g.6329dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*105dup MANE Select ENSP00000328181.4:n.*105dup
ENST00000332822.4:c.*105dup ENSP00000328181.4:n.*105dup
NM_005450.4:c.*105dup NP_005441.1:n.*105dup
NM_005450.6:c.*105dup MANE Select NP_005441.1:n.*105dup