Canonical Allele Identifier: CA363276732
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1223900525
gnomAD v2: 6-24145876-A-G
gnomAD v4: 6-24145648-A-G
MyVariant Identifiers: chr6:g.24145876A>G (hg19) chr6:g.24145648A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145648A>G , CM000668.2:g.24145648A>G GRCh38
NC_000006.11:g.24145876A>G , CM000668.1:g.24145876A>G GRCh37
NC_000006.10:g.24253855A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.290A>G MANE Select ENSP00000367752.4:p.Asp97Gly
ENST00000378477.2:c.290A>G ENSP00000367738.2:p.Asp97Gly
ENST00000378478.5:c.290A>G ENSP00000367739.2:p.Asp97Gly
ENST00000378491.8:c.290A>G ENSP00000367752.4:p.Asp97Gly
ENST00000468195.2:n.257-9123A>G
NM_080723.4:c.290A>G NP_542454.3:p.Asp97Gly
NM_080723.5:c.290A>G MANE Select NP_542454.3:p.Asp97Gly
Search 100 bp 5'
Search 100 bp 3'