Canonical Allele Identifier: CA2266876518
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs2052475170
gnomAD v4: 17-56595078-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595078T>G , CM000679.2:g.56595078T>G GRCh38
NC_000017.10:g.54672439T>G , CM000679.1:g.54672439T>G GRCh37
NC_000017.9:g.52027438T>G NCBI36
NG_011958.1:g.6380T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*156T>G MANE Select ENSP00000328181.4:n.*156T>G
ENST00000332822.4:c.*156T>G ENSP00000328181.4:n.*156T>G
NM_005450.4:c.*156T>G NP_005441.1:n.*156T>G
NM_005450.6:c.*156T>G MANE Select NP_005441.1:n.*156T>G
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