Linked Data
dbSNP Id:
rs1752367240
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111072481del , CM000667.2:g.111072481del | GRCh38 |
| NC_000005.9:g.110408179del , CM000667.1:g.110408179del | GRCh37 |
| NC_000005.8:g.110436078del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344895.4:c.172-407del MANE Select | ENSP00000339804.3:n.172-407del | |
| ENST00000344895.3:c.172-407del | ENSP00000339804.3:n.172-407del | |
| ENST00000420978.6:c.172-407del | ENSP00000399099.2:n.172-407del | |
| NM_033035.4:c.172-407del | NP_149024.1:n.172-407del | |
| NR_045089.1:n.1576-407del | ||
| NM_033035.5:c.172-407del MANE Select | NP_149024.1:n.172-407del | |
| NR_045089.2:n.1594-407del |