Canonical Allele Identifier: CA8663208
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs758969125

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594675C>G , CM000679.2:g.56594675C>G GRCh38
NC_000017.10:g.54672036C>G , CM000679.1:g.54672036C>G GRCh37
NC_000017.9:g.52027035C>G NCBI36
NG_011958.1:g.5977C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.452C>G MANE Select ENSP00000328181.4:p.Ser151Trp
ENST00000332822.4:c.452C>G ENSP00000328181.4:p.Ser151Trp
NM_005450.4:c.452C>G NP_005441.1:p.Ser151Trp
NM_005450.6:c.452C>G MANE Select NP_005441.1:p.Ser151Trp