Canonical Allele Identifier: CA292532935
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs1054982121
MyVariant Identifiers: chr17:g.54672456G>A (hg19) chr17:g.56595095G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595095G>A , CM000679.2:g.56595095G>A GRCh38
NC_000017.10:g.54672456G>A , CM000679.1:g.54672456G>A GRCh37
NC_000017.9:g.52027455G>A NCBI36
NG_011958.1:g.6397G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*173G>A MANE Select ENSP00000328181.4:n.*173G>A
ENST00000332822.4:c.*173G>A ENSP00000328181.4:n.*173G>A
NM_005450.4:c.*173G>A NP_005441.1:n.*173G>A
NM_005450.6:c.*173G>A MANE Select NP_005441.1:n.*173G>A
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