Canonical Allele Identifier: CA2638880938
Gene: NOG HGNC NCBI

Linked Data

gnomAD v4: 17-56594934-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594934C>T , CM000679.2:g.56594934C>T GRCh38
NC_000017.10:g.54672295C>T , CM000679.1:g.54672295C>T GRCh37
NC_000017.9:g.52027294C>T NCBI36
NG_011958.1:g.6236C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*12C>T MANE Select ENSP00000328181.4:n.*12C>T
ENST00000332822.4:c.*12C>T ENSP00000328181.4:n.*12C>T
NM_005450.4:c.*12C>T NP_005441.1:n.*12C>T
NM_005450.6:c.*12C>T MANE Select NP_005441.1:n.*12C>T
Search 100 bp 5'
Search 100 bp 3'