Canonical Allele Identifier: CA2638880962
Gene: NOG HGNC NCBI

Linked Data

gnomAD v4: 17-56594958-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594958A>G , CM000679.2:g.56594958A>G GRCh38
NC_000017.10:g.54672319A>G , CM000679.1:g.54672319A>G GRCh37
NC_000017.9:g.52027318A>G NCBI36
NG_011958.1:g.6260A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*36A>G MANE Select ENSP00000328181.4:n.*36A>G
ENST00000332822.4:c.*36A>G ENSP00000328181.4:n.*36A>G
NM_005450.4:c.*36A>G NP_005441.1:n.*36A>G
NM_005450.6:c.*36A>G MANE Select NP_005441.1:n.*36A>G
Search 100 bp 5'
Search 100 bp 3'