Canonical Allele Identifier: CA2266876498
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs2052474709

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595054T>G , CM000679.2:g.56595054T>G GRCh38
NC_000017.10:g.54672415T>G , CM000679.1:g.54672415T>G GRCh37
NC_000017.9:g.52027414T>G NCBI36
NG_011958.1:g.6356T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*132T>G MANE Select ENSP00000328181.4:n.*132T>G
ENST00000332822.4:c.*132T>G ENSP00000328181.4:n.*132T>G
NM_005450.4:c.*132T>G NP_005441.1:n.*132T>G
NM_005450.6:c.*132T>G MANE Select NP_005441.1:n.*132T>G