Canonical Allele Identifier: CA363276628
Gene: NRSN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24145825T>G (hg19) chr6:g.24145597T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145597T>G , CM000668.2:g.24145597T>G GRCh38
NC_000006.11:g.24145825T>G , CM000668.1:g.24145825T>G GRCh37
NC_000006.10:g.24253804T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.239T>G MANE Select ENSP00000367752.4:p.Leu80Arg
ENST00000378477.2:c.239T>G ENSP00000367738.2:p.Leu80Arg
ENST00000378478.5:c.239T>G ENSP00000367739.2:p.Leu80Arg
ENST00000378491.8:c.239T>G ENSP00000367752.4:p.Leu80Arg
ENST00000468195.2:n.257-9174T>G
NM_080723.4:c.239T>G NP_542454.3:p.Leu80Arg
NM_080723.5:c.239T>G MANE Select NP_542454.3:p.Leu80Arg
Search 100 bp 5'
Search 100 bp 3'