Canonical Allele Identifier: CA399966743
Gene: NOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.54672213G>C (hg19) chr17:g.56594852G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594852G>C , CM000679.2:g.56594852G>C GRCh38
NC_000017.10:g.54672213G>C , CM000679.1:g.54672213G>C GRCh37
NC_000017.9:g.52027212G>C NCBI36
NG_011958.1:g.6154G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000332822.6:c.629G>C MANE Select ENSP00000328181.4:p.Arg210Pro
ENST00000332822.4:c.629G>C ENSP00000328181.4:p.Arg210Pro
NM_005450.4:c.629G>C NP_005441.1:p.Arg210Pro
NM_005450.6:c.629G>C MANE Select NP_005441.1:p.Arg210Pro
Search 100 bp 5'
Search 100 bp 3'