Canonical Allele Identifier: CA984892726
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs2052474016
gnomAD v3: 17-56595024-C-A
gnomAD v4: 17-56595024-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595024C>A , CM000679.2:g.56595024C>A GRCh38
NC_000017.10:g.54672385C>A , CM000679.1:g.54672385C>A GRCh37
NC_000017.9:g.52027384C>A NCBI36
NG_011958.1:g.6326C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*102C>A MANE Select ENSP00000328181.4:n.*102C>A
ENST00000332822.4:c.*102C>A ENSP00000328181.4:n.*102C>A
NM_005450.4:c.*102C>A NP_005441.1:n.*102C>A
NM_005450.6:c.*102C>A MANE Select NP_005441.1:n.*102C>A
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