gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.81151881 (NFE)
Genomes Max Group AF
0.81151881 (NFE)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.97169185A>G , CM000672.2:g.97169185A>G | GRCh38 |
| NC_000010.10:g.98928942A>G , CM000672.1:g.98928942A>G | GRCh37 |
| NC_000010.9:g.98918932A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266058.9:c.198-4295T>C (SLIT1) MANE Select | ENSP00000266058.4:n.198-4295T>C | |
| ENST00000266058.8:c.198-4295T>C (SLIT1) | ENSP00000266058.4:n.198-4295T>C | |
| ENST00000314867.9:c.147-4295T>C (SLIT1) | ENSP00000315005.5:n.147-4295T>C | |
| ENST00000371041.3:c.198-4295T>C (SLIT1) | ENSP00000360080.3:n.198-4295T>C | |
| ENST00000371070.8:c.198-4295T>C (SLIT1) | ENSP00000360109.4:n.198-4295T>C | |
| ENST00000456008.2:n.377-4295T>C (SLIT1) | ||
| ENST00000479633.2:c.1475-4295T>C (ARHGAP19-SLIT1) | ENSP00000473567.1:n.1475-4295T>C | |
| NM_003061.2:c.198-4295T>C (SLIT1) | NP_003052.2:n.198-4295T>C | |
| NR_037909.1:n.1521-4295T>C (ARHGAP19-SLIT1) | ||
| NM_003061.3:c.198-4295T>C (SLIT1) MANE Select | NP_003052.2:n.198-4295T>C |