Canonical Allele Identifier: CA2266876545
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs1839417531

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595121T>G , CM000679.2:g.56595121T>G GRCh38
NC_000017.10:g.54672482T>G , CM000679.1:g.54672482T>G GRCh37
NC_000017.9:g.52027481T>G NCBI36
NG_011958.1:g.6423T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*199T>G MANE Select ENSP00000328181.4:n.*199T>G
ENST00000332822.4:c.*199T>G ENSP00000328181.4:n.*199T>G
NM_005450.4:c.*199T>G NP_005441.1:n.*199T>G
NM_005450.6:c.*199T>G MANE Select NP_005441.1:n.*199T>G