Canonical Allele Identifier: CA118425
Gene: NOG HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6691
dbSNP Id: rs104894602

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594888A>G , CM000679.2:g.56594888A>G GRCh38
NC_000017.10:g.54672249A>G , CM000679.1:g.54672249A>G GRCh37
NC_000017.9:g.52027248A>G NCBI36
NG_011958.1:g.6190A>G

Transcript Alleles

HGVS Amino-acid change
NM_005450.4:c.665A>G VV NP_005441.1:p.Tyr222Cys
ENST00000332822.4:c.665A>G ENSP00000328181.4:p.Tyr222Cys