Canonical Allele Identifier: CA3654353
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs764026713
ExAC: 6:24145889 C / T
gnomAD v2: 6-24145889-C-T
gnomAD v3: 6-24145661-C-T
gnomAD v4: 6-24145661-C-T
MyVariant Identifiers: chr6:g.24145889C>T (hg19) chr6:g.24145661C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145661C>T , CM000668.2:g.24145661C>T GRCh38
NC_000006.11:g.24145889C>T , CM000668.1:g.24145889C>T GRCh37
NC_000006.10:g.24253868C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.303C>T MANE Select ENSP00000367752.4:p.Val101=
ENST00000378477.2:c.303C>T ENSP00000367738.2:p.Val101=
ENST00000378478.5:c.303C>T ENSP00000367739.2:p.Val101=
ENST00000378491.8:c.303C>T ENSP00000367752.4:p.Val101=
ENST00000468195.2:n.257-9110C>T
NM_080723.4:c.303C>T NP_542454.3:p.Val101=
NM_080723.5:c.303C>T MANE Select NP_542454.3:p.Val101=
Search 100 bp 5'
Search 100 bp 3'