Canonical Allele Identifier: CA984892671
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs1334116973

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594947C>G , CM000679.2:g.56594947C>G GRCh38
NC_000017.10:g.54672308C>G , CM000679.1:g.54672308C>G GRCh37
NC_000017.9:g.52027307C>G NCBI36
NG_011958.1:g.6249C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*25C>G MANE Select ENSP00000328181.4:n.*25C>G
ENST00000332822.4:c.*25C>G ENSP00000328181.4:n.*25C>G
NM_005450.4:c.*25C>G NP_005441.1:n.*25C>G
NM_005450.6:c.*25C>G MANE Select NP_005441.1:n.*25C>G