Canonical Allele Identifier: CA2266876092
Gene: NOG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594232C= , CM000679.2:g.56594232C= GRCh38
NC_000017.10:g.54671593C= , CM000679.1:g.54671593C= GRCh37
NC_000017.9:g.52026592C= NCBI36
NG_011958.1:g.5534C=

Transcript Alleles

HGVS Amino-acid change
ENST00000332822.6:c.9C= MANE Select ENSP00000328181.4:p.Arg3=
ENST00000332822.4:c.9C= ENSP00000328181.4:p.Arg3=
NM_005450.4:c.9C= NP_005441.1:p.Arg3=
NM_005450.6:c.9C= MANE Select NP_005441.1:p.Arg3=
Search 100 bp 5'
Search 100 bp 3'