Linked Data
dbSNP Id:
rs1832752296
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.1410708_1410715del , CM000672.2:g.1410708_1410715del | GRCh38 |
| NC_000010.10:g.1452903_1452910del , CM000672.1:g.1452903_1452910del | GRCh37 |
| NC_000010.9:g.1442903_1442910del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381312.6:c.101-31552_101-31545del MANE Select | ENSP00000370713.1:n.101-31552_101-31545del | |
| ENST00000381312.5:c.101-31552_101-31545del | ENSP00000370713.1:n.101-31552_101-31545del | |
| NM_018702.3:c.101-31552_101-31545del | NP_061172.1:n.101-31552_101-31545del | |
| XR_930468.1:n.449-31552_449-31545del | ||
| NM_018702.4:c.101-31552_101-31545del MANE Select | NP_061172.1:n.101-31552_101-31545del |