Canonical Allele Identifier: CA292532942
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs936656350
gnomAD v2: 17-54672527-G-T
gnomAD v3: 17-56595166-G-T
gnomAD v4: 17-56595166-G-T
MyVariant Identifiers: chr17:g.54672527G>T (hg19) chr17:g.56595166G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595166G>T , CM000679.2:g.56595166G>T GRCh38
NC_000017.10:g.54672527G>T , CM000679.1:g.54672527G>T GRCh37
NC_000017.9:g.52027526G>T NCBI36
NG_011958.1:g.6468G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*244G>T MANE Select ENSP00000328181.4:n.*244G>T
ENST00000332822.4:c.*244G>T ENSP00000328181.4:n.*244G>T
NM_005450.4:c.*244G>T NP_005441.1:n.*244G>T
NM_005450.6:c.*244G>T MANE Select NP_005441.1:n.*244G>T
Search 100 bp 5'
Search 100 bp 3'