Canonical Allele Identifier: CA500753569
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs2052474172
gnomAD v3: 17-56595030-AC-A
gnomAD v4: 17-56595030-AC-A
MyVariant Identifiers: chr17:g.54672392del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595031del , CM000679.2:g.56595031del GRCh38
NC_000017.10:g.54672392del , CM000679.1:g.54672392del GRCh37
NC_000017.9:g.52027391del NCBI36
NG_011958.1:g.6333del

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*109del MANE Select ENSP00000328181.4:n.*109del
ENST00000332822.4:c.*109del ENSP00000328181.4:n.*109del
NM_005450.4:c.*109del NP_005441.1:n.*109del
NM_005450.6:c.*109del MANE Select NP_005441.1:n.*109del
Search 100 bp 5'
Search 100 bp 3'