Linked Data
dbSNP Id:
rs11078697
gnomAD v2:
17-7469229-C-T
gnomAD v3:
17-7565912-C-T
gnomAD v4:
17-7565912-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7565912C>T , CM000679.2:g.7565912C>T | GRCh38 |
| NC_000017.10:g.7469229C>T , CM000679.1:g.7469229C>T | GRCh37 |
| NC_000017.9:g.7409953C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000321337.12:c.1263+148C>T (SENP3) MANE Select | ENSP00000314029.8:n.1263+148C>T | |
| ENST00000321337.11:c.1263+148C>T (SENP3) | ENSP00000314029.8:n.1263+148C>T | |
| ENST00000429205.6:c.1263+148C>T (SENP3) | ENSP00000403712.2:n.1263+148C>T | |
| ENST00000580231.5:c.330+148C>T (SENP3) | ENSP00000463358.1:n.330+148C>T | |
| ENST00000580997.1:n.540C>T (SENP3) | ||
| ENST00000583277.1:n.1457C>T (SENP3) | ||
| ENST00000614237.1:c.1053+148C>T (SENP3-EIF4A1) | ENSP00000483614.1:n.1053+148C>T | |
| ENST00000619785.1:c.194+148C>T (SENP3) | ||
| NM_015670.5:c.1263+148C>T (SENP3) | NP_056485.2:n.1263+148C>T | |
| NR_037926.1:n.1546+148C>T (SENP3-EIF4A1) | ||
| NM_015670.6:c.1263+148C>T (SENP3) MANE Select | NP_056485.2:n.1263+148C>T |