Canonical Allele Identifier: CA399966044
Gene: NOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.54671989G>T (hg19) chr17:g.56594628G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594628G>T , CM000679.2:g.56594628G>T GRCh38
NC_000017.10:g.54671989G>T , CM000679.1:g.54671989G>T GRCh37
NC_000017.9:g.52026988G>T NCBI36
NG_011958.1:g.5930G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.405G>T MANE Select ENSP00000328181.4:p.Gln135His
ENST00000332822.4:c.405G>T ENSP00000328181.4:p.Gln135His
NM_005450.4:c.405G>T NP_005441.1:p.Gln135His
NM_005450.6:c.405G>T MANE Select NP_005441.1:p.Gln135His
Search 100 bp 5'
Search 100 bp 3'