Canonical Allele Identifier: CA2638880981
Gene: NOG HGNC NCBI

Linked Data

gnomAD v4: 17-56594982-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594982C>A , CM000679.2:g.56594982C>A GRCh38
NC_000017.10:g.54672343C>A , CM000679.1:g.54672343C>A GRCh37
NC_000017.9:g.52027342C>A NCBI36
NG_011958.1:g.6284C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*60C>A MANE Select ENSP00000328181.4:n.*60C>A
ENST00000332822.4:c.*60C>A ENSP00000328181.4:n.*60C>A
NM_005450.4:c.*60C>A NP_005441.1:n.*60C>A
NM_005450.6:c.*60C>A MANE Select NP_005441.1:n.*60C>A
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