Canonical Allele Identifier: CA500985232
Gene: NOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.54671887G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594526G>C , CM000679.2:g.56594526G>C GRCh38
NC_000017.10:g.54671887G>C , CM000679.1:g.54671887G>C GRCh37
NC_000017.9:g.52026886G>C NCBI36
NG_011958.1:g.5828G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000332822.6:c.303G>C MANE Select ENSP00000328181.4:p.Leu101=
ENST00000332822.4:c.303G>C ENSP00000328181.4:p.Leu101=
NM_005450.4:c.303G>C NP_005441.1:p.Leu101=
NM_005450.6:c.303G>C MANE Select NP_005441.1:p.Leu101=
Search 100 bp 5'
Search 100 bp 3'