Canonical Allele Identifier: CA399966520
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594747T>C , CM000679.2:g.56594747T>C GRCh38
NC_000017.10:g.54672108T>C , CM000679.1:g.54672108T>C GRCh37
NC_000017.9:g.52027107T>C NCBI36
NG_011958.1:g.6049T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000332822.6:c.524T>C MANE Select ENSP00000328181.4:p.Val175Ala
ENST00000332822.4:c.524T>C ENSP00000328181.4:p.Val175Ala
NM_005450.4:c.524T>C NP_005441.1:p.Val175Ala
NM_005450.6:c.524T>C MANE Select NP_005441.1:p.Val175Ala