Canonical Allele Identifier: CA500753570
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs2052475050
gnomAD v4: 17-56595073-C-G
MyVariant Identifiers: chr17:g.54672434C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595073C>G , CM000679.2:g.56595073C>G GRCh38
NC_000017.10:g.54672434C>G , CM000679.1:g.54672434C>G GRCh37
NC_000017.9:g.52027433C>G NCBI36
NG_011958.1:g.6375C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*151C>G MANE Select ENSP00000328181.4:n.*151C>G
ENST00000332822.4:c.*151C>G ENSP00000328181.4:n.*151C>G
NM_005450.4:c.*151C>G NP_005441.1:n.*151C>G
NM_005450.6:c.*151C>G MANE Select NP_005441.1:n.*151C>G
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