Canonical Allele Identifier: CA399965580
Gene: NOG HGNC NCBI

Linked Data

gnomAD v4: 17-56594530-G-A
MyVariant Identifiers: chr17:g.54671891G>A (hg19) chr17:g.56594530G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594530G>A , CM000679.2:g.56594530G>A GRCh38
NC_000017.10:g.54671891G>A , CM000679.1:g.54671891G>A GRCh37
NC_000017.9:g.52026890G>A NCBI36
NG_011958.1:g.5832G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000332822.6:c.307G>A MANE Select ENSP00000328181.4:p.Glu103Lys
ENST00000332822.4:c.307G>A ENSP00000328181.4:p.Glu103Lys
NM_005450.4:c.307G>A NP_005441.1:p.Glu103Lys
NM_005450.6:c.307G>A MANE Select NP_005441.1:p.Glu103Lys
Search 100 bp 5'
Search 100 bp 3'