Canonical Allele Identifier: CA363276690
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs199771455
gnomAD v2: 6-24145857-G-T
gnomAD v3: 6-24145629-G-T
gnomAD v4: 6-24145629-G-T
MyVariant Identifiers: chr6:g.24145857G>T (hg19) chr6:g.24145629G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145629G>T , CM000668.2:g.24145629G>T GRCh38
NC_000006.11:g.24145857G>T , CM000668.1:g.24145857G>T GRCh37
NC_000006.10:g.24253836G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.271G>T MANE Select ENSP00000367752.4:p.Glu91Ter
ENST00000378477.2:c.271G>T ENSP00000367738.2:p.Glu91Ter
ENST00000378478.5:c.271G>T ENSP00000367739.2:p.Glu91Ter
ENST00000378491.8:c.271G>T ENSP00000367752.4:p.Glu91Ter
ENST00000468195.2:n.257-9142G>T
NM_080723.4:c.271G>T NP_542454.3:p.Glu91Ter
NM_080723.5:c.271G>T MANE Select NP_542454.3:p.Glu91Ter
Search 100 bp 5'
Search 100 bp 3'