Canonical Allele Identifier: CA8663180
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs770837708

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594526G>A , CM000679.2:g.56594526G>A GRCh38
NC_000017.10:g.54671887G>A , CM000679.1:g.54671887G>A GRCh37
NC_000017.9:g.52026886G>A NCBI36
NG_011958.1:g.5828G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.303G>A MANE Select ENSP00000328181.4:p.Leu101=
ENST00000332822.4:c.303G>A ENSP00000328181.4:p.Leu101=
NM_005450.4:c.303G>A NP_005441.1:p.Leu101=
NM_005450.6:c.303G>A MANE Select NP_005441.1:p.Leu101=