Canonical Allele Identifier: CA1616315638
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1760284229
gnomAD v3: 6-24145266-T-C
gnomAD v4: 6-24145266-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145266T>C , CM000668.2:g.24145266T>C GRCh38
NC_000006.11:g.24145494T>C , CM000668.1:g.24145494T>C GRCh37
NC_000006.10:g.24253473T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.190-282T>C MANE Select ENSP00000367752.4:n.190-282T>C
ENST00000378477.2:c.190-282T>C ENSP00000367738.2:n.190-282T>C
ENST00000378478.5:c.190-282T>C ENSP00000367739.2:n.190-282T>C
ENST00000378491.8:c.190-282T>C ENSP00000367752.4:n.190-282T>C
ENST00000468195.2:n.257-9505T>C
NM_080723.4:c.190-282T>C NP_542454.3:n.190-282T>C
NM_080723.5:c.190-282T>C MANE Select NP_542454.3:n.190-282T>C
Search 100 bp 5'
Search 100 bp 3'