Canonical Allele Identifier: CA2266876551
Gene: NOG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595128G= , CM000679.2:g.56595128G= GRCh38
NC_000017.10:g.54672489G= , CM000679.1:g.54672489G= GRCh37
NC_000017.9:g.52027488G= NCBI36
NG_011958.1:g.6430G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*206G= MANE Select ENSP00000328181.4:n.*206G=
ENST00000332822.4:c.*206G= ENSP00000328181.4:n.*206G=
NM_005450.4:c.*206G= NP_005441.1:n.*206G=
NM_005450.6:c.*206G= MANE Select NP_005441.1:n.*206G=
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