Canonical Allele Identifier: CA363277231
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1187787282
MyVariant Identifiers: chr6:g.24146104G>C (hg19) chr6:g.24145876G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145876G>C , CM000668.2:g.24145876G>C GRCh38
NC_000006.11:g.24146104G>C , CM000668.1:g.24146104G>C GRCh37
NC_000006.10:g.24254083G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.518G>C MANE Select ENSP00000367752.4:p.Gly173Ala
ENST00000378477.2:c.518G>C
ENST00000378478.5:c.518G>C ENSP00000367739.2:p.Gly173Ala
ENST00000378491.8:c.518G>C ENSP00000367752.4:p.Gly173Ala
ENST00000468195.2:n.257-8895G>C
NM_080723.4:c.518G>C NP_542454.3:p.Gly173Ala
NM_080723.5:c.518G>C MANE Select NP_542454.3:p.Gly173Ala
Search 100 bp 5'
Search 100 bp 3'