Canonical Allele Identifier: CA2809927367
Gene: NOG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595160T>G , CM000679.2:g.56595160T>G GRCh38
NC_000017.10:g.54672521T>G , CM000679.1:g.54672521T>G GRCh37
NC_000017.9:g.52027520T>G NCBI36
NG_011958.1:g.6462T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*238T>G MANE Select ENSP00000328181.4:n.*238T>G
ENST00000332822.4:c.*238T>G ENSP00000328181.4:n.*238T>G
NM_005450.4:c.*238T>G NP_005441.1:n.*238T>G
NM_005450.6:c.*238T>G MANE Select NP_005441.1:n.*238T>G
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