Canonical Allele Identifier: CA399966166
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594672G>C , CM000679.2:g.56594672G>C GRCh38
NC_000017.10:g.54672033G>C , CM000679.1:g.54672033G>C GRCh37
NC_000017.9:g.52027032G>C NCBI36
NG_011958.1:g.5974G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.449G>C MANE Select ENSP00000328181.4:p.Trp150Ser
ENST00000332822.4:c.449G>C ENSP00000328181.4:p.Trp150Ser
NM_005450.4:c.449G>C NP_005441.1:p.Trp150Ser
NM_005450.6:c.449G>C MANE Select NP_005441.1:p.Trp150Ser