Canonical Allele Identifier: CA399966318

Gene: NOG

Linked Data

• MyVariant Identifiers: chr17:g.54672065T>G (hg19) ; chr17:g.56594704T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56594704T>G , CM000679.2:g.56594704T>G	GRCh38
NC_000017.10:g.54672065T>G , CM000679.1:g.54672065T>G	GRCh37
NC_000017.9:g.52027064T>G	NCBI36
NG_011958.1:g.6006T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.481T>G MANE Select	ENSP00000328181.4:p.Trp161Gly
ENST00000332822.4:c.481T>G	ENSP00000328181.4:p.Trp161Gly
NM_005450.4:c.481T>G	NP_005441.1:p.Trp161Gly
NM_005450.6:c.481T>G MANE Select	NP_005441.1:p.Trp161Gly