Linked Data
dbSNP Id:
rs2092588632
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149926101_149926110del , CM000663.2:g.149926101_149926110del | GRCh38 |
| NC_000001.10:g.149897993_149898002del , CM000663.1:g.149897993_149898002del | GRCh37 |
| NC_000001.9:g.148164617_148164626del | NCBI36 |
| NG_032777.1:g.7143_7152del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.9:c.707-68_707-59del MANE Select | ENSP00000271628.8:n.707-68_707-59del | |
| ENST00000271628.8:c.707-68_707-59del | ENSP00000271628.8:n.707-68_707-59del | |
| NM_005850.4:c.707-68_707-59del | NP_005841.1:n.707-68_707-59del | |
| NM_005850.5:c.707-68_707-59del MANE Select | NP_005841.1:n.707-68_707-59del |