Canonical Allele Identifier: CA2266876427
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594963T= , CM000679.2:g.56594963T= GRCh38
NC_000017.10:g.54672324T= , CM000679.1:g.54672324T= GRCh37
NC_000017.9:g.52027323T= NCBI36
NG_011958.1:g.6265T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*41T= MANE Select ENSP00000328181.4:n.*41T=
ENST00000332822.4:c.*41T= ENSP00000328181.4:n.*41T=
NM_005450.4:c.*41T= NP_005441.1:n.*41T=
NM_005450.6:c.*41T= MANE Select NP_005441.1:n.*41T=