Canonical Allele Identifier: CA2638881145
Gene: NOG HGNC NCBI

Linked Data

gnomAD v4: 17-56595152-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595152T>A , CM000679.2:g.56595152T>A GRCh38
NC_000017.10:g.54672513T>A , CM000679.1:g.54672513T>A GRCh37
NC_000017.9:g.52027512T>A NCBI36
NG_011958.1:g.6454T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*230T>A MANE Select ENSP00000328181.4:n.*230T>A
ENST00000332822.4:c.*230T>A ENSP00000328181.4:n.*230T>A
NM_005450.4:c.*230T>A NP_005441.1:n.*230T>A
NM_005450.6:c.*230T>A MANE Select NP_005441.1:n.*230T>A
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