Canonical Allele Identifier: CA399966155
Gene: NOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.54672030T>C (hg19) chr17:g.56594669T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594669T>C , CM000679.2:g.56594669T>C GRCh38
NC_000017.10:g.54672030T>C , CM000679.1:g.54672030T>C GRCh37
NC_000017.9:g.52027029T>C NCBI36
NG_011958.1:g.5971T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.446T>C MANE Select ENSP00000328181.4:p.Leu149Pro
ENST00000332822.4:c.446T>C ENSP00000328181.4:p.Leu149Pro
NM_005450.4:c.446T>C NP_005441.1:p.Leu149Pro
NM_005450.6:c.446T>C MANE Select NP_005441.1:p.Leu149Pro
Search 100 bp 5'
Search 100 bp 3'