Canonical Allele Identifier: CA823264994
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1304425710
gnomAD v3: 6-24145263-C-A
gnomAD v4: 6-24145263-C-A
MyVariant Identifiers: chr6:g.24145491C>A (hg19) chr6:g.24145263C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145263C>A , CM000668.2:g.24145263C>A GRCh38
NC_000006.11:g.24145491C>A , CM000668.1:g.24145491C>A GRCh37
NC_000006.10:g.24253470C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.190-285C>A MANE Select ENSP00000367752.4:n.190-285C>A
ENST00000378477.2:c.190-285C>A ENSP00000367738.2:n.190-285C>A
ENST00000378478.5:c.190-285C>A ENSP00000367739.2:n.190-285C>A
ENST00000378491.8:c.190-285C>A ENSP00000367752.4:n.190-285C>A
ENST00000468195.2:n.257-9508C>A
NM_080723.4:c.190-285C>A NP_542454.3:n.190-285C>A
NM_080723.5:c.190-285C>A MANE Select NP_542454.3:n.190-285C>A
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