Canonical Allele Identifier: CA399966492
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594740G>C , CM000679.2:g.56594740G>C GRCh38
NC_000017.10:g.54672101G>C , CM000679.1:g.54672101G>C GRCh37
NC_000017.9:g.52027100G>C NCBI36
NG_011958.1:g.6042G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000332822.6:c.517G>C MANE Select ENSP00000328181.4:p.Val173Leu
ENST00000332822.4:c.517G>C ENSP00000328181.4:p.Val173Leu
NM_005450.4:c.517G>C NP_005441.1:p.Val173Leu
NM_005450.6:c.517G>C MANE Select NP_005441.1:p.Val173Leu