Canonical Allele Identifier: CA136618336
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1025494234
gnomAD v3: 6-24146019-A-T
gnomAD v4: 6-24146019-A-T
MyVariant Identifiers: chr6:g.24146247A>T (hg19) chr6:g.24146019A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24146019A>T , CM000668.2:g.24146019A>T GRCh38
NC_000006.11:g.24146247A>T , CM000668.1:g.24146247A>T GRCh37
NC_000006.10:g.24254226A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.*73A>T MANE Select ENSP00000367752.4:n.*73A>T
ENST00000378478.5:c.*73A>T ENSP00000367739.2:n.*73A>T
ENST00000378491.8:c.*73A>T ENSP00000367752.4:n.*73A>T
ENST00000468195.2:n.257-8752A>T
NM_080723.4:c.*73A>T NP_542454.3:n.*73A>T
NM_080723.5:c.*73A>T MANE Select NP_542454.3:n.*73A>T
Search 100 bp 5'
Search 100 bp 3'