Canonical Allele Identifier: CA399967004
Gene: NOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.54672278T>A (hg19) chr17:g.56594917T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594917T>A , CM000679.2:g.56594917T>A GRCh38
NC_000017.10:g.54672278T>A , CM000679.1:g.54672278T>A GRCh37
NC_000017.9:g.52027277T>A NCBI36
NG_011958.1:g.6219T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.694T>A MANE Select ENSP00000328181.4:p.Cys232Ser
ENST00000332822.4:c.694T>A ENSP00000328181.4:p.Cys232Ser
NM_005450.4:c.694T>A NP_005441.1:p.Cys232Ser
NM_005450.6:c.694T>A MANE Select NP_005441.1:p.Cys232Ser
Search 100 bp 5'
Search 100 bp 3'