Canonical Allele Identifier: CA448963089
Gene: NRSN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24145865T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145637T>C , CM000668.2:g.24145637T>C GRCh38
NC_000006.11:g.24145865T>C , CM000668.1:g.24145865T>C GRCh37
NC_000006.10:g.24253844T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.279T>C MANE Select ENSP00000367752.4:p.Phe93=
ENST00000378477.2:c.279T>C ENSP00000367738.2:p.Phe93=
ENST00000378478.5:c.279T>C ENSP00000367739.2:p.Phe93=
ENST00000378491.8:c.279T>C ENSP00000367752.4:p.Phe93=
ENST00000468195.2:n.257-9134T>C
NM_080723.4:c.279T>C NP_542454.3:p.Phe93=
NM_080723.5:c.279T>C MANE Select NP_542454.3:p.Phe93=
Search 100 bp 5'
Search 100 bp 3'