Canonical Allele Identifier: CA292532943
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs1052727668
gnomAD v3: 17-56595185-A-C
gnomAD v4: 17-56595185-A-C
MyVariant Identifiers: chr17:g.54672546A>C (hg19) chr17:g.56595185A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595185A>C , CM000679.2:g.56595185A>C GRCh38
NC_000017.10:g.54672546A>C , CM000679.1:g.54672546A>C GRCh37
NC_000017.9:g.52027545A>C NCBI36
NG_011958.1:g.6487A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*263A>C MANE Select ENSP00000328181.4:n.*263A>C
ENST00000332822.4:c.*263A>C ENSP00000328181.4:n.*263A>C
NM_005450.4:c.*263A>C NP_005441.1:n.*263A>C
NM_005450.6:c.*263A>C MANE Select NP_005441.1:n.*263A>C
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