Canonical Allele Identifier: CA2266876344
Gene: NOG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594779G= , CM000679.2:g.56594779G= GRCh38
NC_000017.10:g.54672140G= , CM000679.1:g.54672140G= GRCh37
NC_000017.9:g.52027139G= NCBI36
NG_011958.1:g.6081G=

Transcript Alleles

HGVS Amino-acid change
ENST00000332822.6:c.556G= MANE Select ENSP00000328181.4:p.Val186=
ENST00000332822.4:c.556G= ENSP00000328181.4:p.Val186=
NM_005450.4:c.556G= NP_005441.1:p.Val186=
NM_005450.6:c.556G= MANE Select NP_005441.1:p.Val186=
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Search 100 bp 3'