Canonical Allele Identifier: CA292532932

Gene: NOG

Linked Data

• dbSNP Id: rs868736739
• MyVariant Identifiers: chr17:g.54672444G>A (hg19) ; chr17:g.56595083G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56595083G>A , CM000679.2:g.56595083G>A	GRCh38
NC_000017.10:g.54672444G>A , CM000679.1:g.54672444G>A	GRCh37
NC_000017.9:g.52027443G>A	NCBI36
NG_011958.1:g.6385G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.*161G>A MANE Select	ENSP00000328181.4:n.*161G>A
ENST00000332822.4:c.*161G>A	ENSP00000328181.4:n.*161G>A
NM_005450.4:c.*161G>A	NP_005441.1:n.*161G>A
NM_005450.6:c.*161G>A MANE Select	NP_005441.1:n.*161G>A