Canonical Allele Identifier: CA2638881132
Gene: NOG HGNC NCBI

Linked Data

gnomAD v4: 17-56595140-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595140T>C , CM000679.2:g.56595140T>C GRCh38
NC_000017.10:g.54672501T>C , CM000679.1:g.54672501T>C GRCh37
NC_000017.9:g.52027500T>C NCBI36
NG_011958.1:g.6442T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*218T>C MANE Select ENSP00000328181.4:n.*218T>C
ENST00000332822.4:c.*218T>C ENSP00000328181.4:n.*218T>C
NM_005450.4:c.*218T>C NP_005441.1:n.*218T>C
NM_005450.6:c.*218T>C MANE Select NP_005441.1:n.*218T>C
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