Canonical Allele Identifier: CA626958025
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs1335121053
gnomAD v2: 17-54672289-G-C
gnomAD v3: 17-56594928-G-C
gnomAD v4: 17-56594928-G-C
MyVariant Identifiers: chr17:g.54672289G>C (hg19) chr17:g.56594928G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594928G>C , CM000679.2:g.56594928G>C GRCh38
NC_000017.10:g.54672289G>C , CM000679.1:g.54672289G>C GRCh37
NC_000017.9:g.52027288G>C NCBI36
NG_011958.1:g.6230G>C

Transcript Alleles

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