Canonical Allele Identifier: CA2677512578
Gene: NRSN1 HGNC NCBI

Linked Data

gnomAD v4: 6-24146051-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24146051G>T , CM000668.2:g.24146051G>T GRCh38
NC_000006.11:g.24146279G>T , CM000668.1:g.24146279G>T GRCh37
NC_000006.10:g.24254258G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.*105G>T MANE Select ENSP00000367752.4:n.*105G>T
ENST00000378478.5:c.*105G>T ENSP00000367739.2:n.*105G>T
ENST00000378491.8:c.*105G>T ENSP00000367752.4:n.*105G>T
ENST00000468195.2:n.257-8720G>T
NM_080723.4:c.*105G>T NP_542454.3:n.*105G>T
NM_080723.5:c.*105G>T MANE Select NP_542454.3:n.*105G>T
Search 100 bp 5'
Search 100 bp 3'