Canonical Allele Identifier: CA8663215
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs778378498

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594758T>C , CM000679.2:g.56594758T>C GRCh38
NC_000017.10:g.54672119T>C , CM000679.1:g.54672119T>C GRCh37
NC_000017.9:g.52027118T>C NCBI36
NG_011958.1:g.6060T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.535T>C MANE Select ENSP00000328181.4:p.Phe179Leu
ENST00000332822.4:c.535T>C ENSP00000328181.4:p.Phe179Leu
NM_005450.4:c.535T>C NP_005441.1:p.Phe179Leu
NM_005450.6:c.535T>C MANE Select NP_005441.1:p.Phe179Leu