Canonical Allele Identifier: CA2266876476
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595025A= , CM000679.2:g.56595025A= GRCh38
NC_000017.10:g.54672386A= , CM000679.1:g.54672386A= GRCh37
NC_000017.9:g.52027385A= NCBI36
NG_011958.1:g.6327A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*103A= MANE Select ENSP00000328181.4:n.*103A=
ENST00000332822.4:c.*103A= ENSP00000328181.4:n.*103A=
NM_005450.4:c.*103A= NP_005441.1:n.*103A=
NM_005450.6:c.*103A= MANE Select NP_005441.1:n.*103A=