Canonical Allele Identifier: CA399966995
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594914T>A , CM000679.2:g.56594914T>A GRCh38
NC_000017.10:g.54672275T>A , CM000679.1:g.54672275T>A GRCh37
NC_000017.9:g.52027274T>A NCBI36
NG_011958.1:g.6216T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.691T>A MANE Select ENSP00000328181.4:p.Ser231Thr
ENST00000332822.4:c.691T>A ENSP00000328181.4:p.Ser231Thr
NM_005450.4:c.691T>A NP_005441.1:p.Ser231Thr
NM_005450.6:c.691T>A MANE Select NP_005441.1:p.Ser231Thr