Canonical Allele Identifier: CA500985506
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs1357240545
gnomAD v4: 17-56594703-G-T
MyVariant Identifiers: chr17:g.54672064G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594703G>T , CM000679.2:g.56594703G>T GRCh38
NC_000017.10:g.54672064G>T , CM000679.1:g.54672064G>T GRCh37
NC_000017.9:g.52027063G>T NCBI36
NG_011958.1:g.6005G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000332822.6:c.480G>T MANE Select ENSP00000328181.4:p.Ala160=
ENST00000332822.4:c.480G>T ENSP00000328181.4:p.Ala160=
NM_005450.4:c.480G>T NP_005441.1:p.Ala160=
NM_005450.6:c.480G>T MANE Select NP_005441.1:p.Ala160=
Search 100 bp 5'
Search 100 bp 3'