Canonical Allele Identifier: CA448963011
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1581554316
MyVariant Identifiers: chr6:g.24145805G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145577G>A , CM000668.2:g.24145577G>A GRCh38
NC_000006.11:g.24145805G>A , CM000668.1:g.24145805G>A GRCh37
NC_000006.10:g.24253784G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378491.9:c.219G>A MANE Select ENSP00000367752.4:p.Val73=
ENST00000378477.2:c.219G>A ENSP00000367738.2:p.Val73=
ENST00000378478.5:c.219G>A ENSP00000367739.2:p.Val73=
ENST00000378491.8:c.219G>A ENSP00000367752.4:p.Val73=
ENST00000468195.2:n.257-9194G>A
NM_080723.4:c.219G>A NP_542454.3:p.Val73=
NM_080723.5:c.219G>A MANE Select NP_542454.3:p.Val73=