Canonical Allele Identifier: CA3654356
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs201114574
gnomAD v2: 6-24145901-T-C
gnomAD v3: 6-24145673-T-C
gnomAD v4: 6-24145673-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145673T>C , CM000668.2:g.24145673T>C GRCh38
NC_000006.11:g.24145901T>C , CM000668.1:g.24145901T>C GRCh37
NC_000006.10:g.24253880T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378491.9:c.315T>C MANE Select ENSP00000367752.4:p.Ala105=
ENST00000378477.2:c.315T>C ENSP00000367738.2:p.Ala105=
ENST00000378478.5:c.315T>C ENSP00000367739.2:p.Ala105=
ENST00000378491.8:c.315T>C ENSP00000367752.4:p.Ala105=
ENST00000468195.2:n.257-9098T>C
NM_080723.4:c.315T>C NP_542454.3:p.Ala105=
NM_080723.5:c.315T>C MANE Select NP_542454.3:p.Ala105=