Canonical Allele Identifier: CA773337101
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs1211439342
gnomAD v3: 17-56595155-A-G
gnomAD v4: 17-56595155-A-G
MyVariant Identifiers: chr17:g.54672516A>G (hg19) chr17:g.56595155A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595155A>G , CM000679.2:g.56595155A>G GRCh38
NC_000017.10:g.54672516A>G , CM000679.1:g.54672516A>G GRCh37
NC_000017.9:g.52027515A>G NCBI36
NG_011958.1:g.6457A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*233A>G MANE Select ENSP00000328181.4:n.*233A>G
ENST00000332822.4:c.*233A>G ENSP00000328181.4:n.*233A>G
NM_005450.4:c.*233A>G NP_005441.1:n.*233A>G
NM_005450.6:c.*233A>G MANE Select NP_005441.1:n.*233A>G
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