Canonical Allele Identifier: CA823265017
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1191701464
MyVariant Identifiers: chr6:g.24145510G>A (hg19) chr6:g.24145282G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145282G>A , CM000668.2:g.24145282G>A GRCh38
NC_000006.11:g.24145510G>A , CM000668.1:g.24145510G>A GRCh37
NC_000006.10:g.24253489G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.190-266G>A MANE Select ENSP00000367752.4:n.190-266G>A
ENST00000378477.2:c.190-266G>A ENSP00000367738.2:n.190-266G>A
ENST00000378478.5:c.190-266G>A ENSP00000367739.2:n.190-266G>A
ENST00000378491.8:c.190-266G>A ENSP00000367752.4:n.190-266G>A
ENST00000468195.2:n.257-9489G>A
NM_080723.4:c.190-266G>A NP_542454.3:n.190-266G>A
NM_080723.5:c.190-266G>A MANE Select NP_542454.3:n.190-266G>A
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