Canonical Allele Identifier: CA2638881115
Gene: NOG HGNC NCBI

Linked Data

gnomAD v4: 17-56595122-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595122A>G , CM000679.2:g.56595122A>G GRCh38
NC_000017.10:g.54672483A>G , CM000679.1:g.54672483A>G GRCh37
NC_000017.9:g.52027482A>G NCBI36
NG_011958.1:g.6424A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*200A>G MANE Select ENSP00000328181.4:n.*200A>G
ENST00000332822.4:c.*200A>G ENSP00000328181.4:n.*200A>G
NM_005450.4:c.*200A>G NP_005441.1:n.*200A>G
NM_005450.6:c.*200A>G MANE Select NP_005441.1:n.*200A>G
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