Canonical Allele Identifier: CA500753552
Gene: NOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.54672253C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594892C>T , CM000679.2:g.56594892C>T GRCh38
NC_000017.10:g.54672253C>T , CM000679.1:g.54672253C>T GRCh37
NC_000017.9:g.52027252C>T NCBI36
NG_011958.1:g.6194C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.669C>T MANE Select ENSP00000328181.4:p.Pro223=
ENST00000332822.4:c.669C>T ENSP00000328181.4:p.Pro223=
NM_005450.4:c.669C>T NP_005441.1:p.Pro223=
NM_005450.6:c.669C>T MANE Select NP_005441.1:p.Pro223=
Search 100 bp 5'
Search 100 bp 3'