Canonical Allele Identifier: CA2266876089

Gene: NOG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56594227G= , CM000679.2:g.56594227G=	GRCh38
NC_000017.10:g.54671588G= , CM000679.1:g.54671588G=	GRCh37
NC_000017.9:g.52026587G=	NCBI36
NG_011958.1:g.5529G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000332822.6:c.4G= MANE Select	ENSP00000328181.4:p.Glu2=
ENST00000332822.4:c.4G=	ENSP00000328181.4:p.Glu2=
NM_005450.4:c.4G=	NP_005441.1:p.Glu2=
NM_005450.6:c.4G= MANE Select	NP_005441.1:p.Glu2=