Canonical Allele Identifier: CA984892718
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs1597920508
gnomAD v3: 17-56595016-A-T
gnomAD v4: 17-56595016-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595016A>T , CM000679.2:g.56595016A>T GRCh38
NC_000017.10:g.54672377A>T , CM000679.1:g.54672377A>T GRCh37
NC_000017.9:g.52027376A>T NCBI36
NG_011958.1:g.6318A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*94A>T MANE Select ENSP00000328181.4:n.*94A>T
ENST00000332822.4:c.*94A>T ENSP00000328181.4:n.*94A>T
NM_005450.4:c.*94A>T NP_005441.1:n.*94A>T
NM_005450.6:c.*94A>T MANE Select NP_005441.1:n.*94A>T
Search 100 bp 5'
Search 100 bp 3'