Linked Data
dbSNP Id:
rs2097481402
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122461762del , CM000672.2:g.122461762del | GRCh38 |
| NC_000010.10:g.124221278del , CM000672.1:g.124221278del | GRCh37 |
| NC_000010.9:g.124211268del | NCBI36 |
| NG_011554.1:g.5238del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000368984.8:c.110del MANE Select | ENSP00000357980.3:p.Cys37SerfsTer? | |
| ENST00000648167.1:c.154+3053del | ENSP00000498033.1:n.154+3053del | |
| ENST00000368984.7:c.110del | ENSP00000357980.3:p.Cys37SerfsTer? | |
| NM_002775.4:c.110del | NP_002766.1:p.Cys37SerfsTer? | |
| NM_002775.5:c.110del MANE Select | NP_002766.1:p.Cys37SerfsTer? |