Linked Data
dbSNP Id:
rs2092288043
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149884938_149884940del , CM000663.2:g.149884938_149884940del | GRCh38 |
| NC_000001.10:g.149856488_149856490del , CM000663.1:g.149856488_149856490del | GRCh37 |
| NC_000001.9:g.148123112_148123114del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369155.4:c.*1322_*1324del MANE Select | ENSP00000358151.2:n.*1322_*1324del | |
| ENST00000369155.3:c.*1322_*1324del | ENSP00000358151.2:n.*1322_*1324del | |
| ENST00000369160.3:c.377+1326_377+1328del | ENSP00000375736.2:n.377+1326_377+1328del | |
| NM_003528.2:c.*1322_*1324del | NP_003519.1:n.*1322_*1324del | |
| NM_003528.3:c.*1322_*1324del MANE Select | NP_003519.1:n.*1322_*1324del |