Canonical Allele Identifier: CA118435
Gene: NOG HGNC NCBI

Linked Data

ClinVar Variation Id: 6702
ClinVar RCV Id: RCV000007092
dbSNP Id: rs121908949

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594722C>G , CM000679.2:g.56594722C>G GRCh38
NC_000017.10:g.54672083C>G , CM000679.1:g.54672083C>G GRCh37
NC_000017.9:g.52027082C>G NCBI36
NG_011958.1:g.6024C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000332822.6:c.499C>G MANE Select ENSP00000328181.4:p.Arg167Gly
ENST00000332822.4:c.499C>G ENSP00000328181.4:p.Arg167Gly
NM_005450.4:c.499C>G NP_005441.1:p.Arg167Gly
NM_005450.6:c.499C>G MANE Select NP_005441.1:p.Arg167Gly