Canonical Allele Identifier: CA448950269
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1388252264
MyVariant Identifiers: chr6:g.24146105G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145877G>T , CM000668.2:g.24145877G>T GRCh38
NC_000006.11:g.24146105G>T , CM000668.1:g.24146105G>T GRCh37
NC_000006.10:g.24254084G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.519G>T MANE Select ENSP00000367752.4:p.Gly173=
ENST00000378478.5:c.519G>T ENSP00000367739.2:p.Gly173=
ENST00000378491.8:c.519G>T ENSP00000367752.4:p.Gly173=
ENST00000468195.2:n.257-8894G>T
NM_080723.4:c.519G>T NP_542454.3:p.Gly173=
NM_080723.5:c.519G>T MANE Select NP_542454.3:p.Gly173=
Search 100 bp 5'
Search 100 bp 3'