Canonical Allele Identifier: CA399966342
Gene: NOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.54672070C>A (hg19) chr17:g.56594709C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594709C>A , CM000679.2:g.56594709C>A GRCh38
NC_000017.10:g.54672070C>A , CM000679.1:g.54672070C>A GRCh37
NC_000017.9:g.52027069C>A NCBI36
NG_011958.1:g.6011C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.486C>A MANE Select ENSP00000328181.4:p.Asn162Lys
ENST00000332822.4:c.486C>A ENSP00000328181.4:p.Asn162Lys
NM_005450.4:c.486C>A NP_005441.1:p.Asn162Lys
NM_005450.6:c.486C>A MANE Select NP_005441.1:p.Asn162Lys
Search 100 bp 5'
Search 100 bp 3'