Canonical Allele Identifier: CA399965955
Gene: NOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.54671960T>C (hg19) chr17:g.56594599T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594599T>C , CM000679.2:g.56594599T>C GRCh38
NC_000017.10:g.54671960T>C , CM000679.1:g.54671960T>C GRCh37
NC_000017.9:g.52026959T>C NCBI36
NG_011958.1:g.5901T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.376T>C MANE Select ENSP00000328181.4:p.Ser126Pro
ENST00000332822.4:c.376T>C ENSP00000328181.4:p.Ser126Pro
NM_005450.4:c.376T>C NP_005441.1:p.Ser126Pro
NM_005450.6:c.376T>C MANE Select NP_005441.1:p.Ser126Pro
Search 100 bp 5'
Search 100 bp 3'