Canonical Allele Identifier: CA2638880967
Gene: NOG HGNC NCBI

Linked Data

gnomAD v4: 17-56594964-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594964C>G , CM000679.2:g.56594964C>G GRCh38
NC_000017.10:g.54672325C>G , CM000679.1:g.54672325C>G GRCh37
NC_000017.9:g.52027324C>G NCBI36
NG_011958.1:g.6266C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*42C>G MANE Select ENSP00000328181.4:n.*42C>G
ENST00000332822.4:c.*42C>G ENSP00000328181.4:n.*42C>G
NM_005450.4:c.*42C>G NP_005441.1:n.*42C>G
NM_005450.6:c.*42C>G MANE Select NP_005441.1:n.*42C>G
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