Canonical Allele Identifier: CA2576328695
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594923A>G , CM000679.2:g.56594923A>G GRCh38
NC_000017.10:g.54672284A>G , CM000679.1:g.54672284A>G GRCh37
NC_000017.9:g.52027283A>G NCBI36
NG_011958.1:g.6225A>G

Transcript Alleles

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