Linked Data
dbSNP Id:
rs1907220629
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30234820_30234821del , CM000679.2:g.30234820_30234821del | GRCh38 |
| NC_000017.10:g.28561838_28561839del , CM000679.1:g.28561838_28561839del | GRCh37 |
| NC_000017.9:g.25585964_25585965del | NCBI36 |
| NG_011747.2:g.6119_6120del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650711.1:c.-221+795_-221+796del MANE Select | ENSP00000498537.1:n.-221+795_-221+796del | |
| ENST00000261707.7:c.-221+795_-221+796del | ENSP00000261707.3:n.-221+795_-221+796del | |
| ENST00000394821.2:c.-221+795_-221+796del | ENSP00000378298.2:n.-221+795_-221+796del | |
| ENST00000401766.6:c.-124+795_-124+796del | ENSP00000385822.2:n.-124+795_-124+796del | |
| NM_001045.5:c.-221+795_-221+796del | NP_001036.1:n.-221+795_-221+796del | |
| NM_001045.6:c.-221+795_-221+796del MANE Select | NP_001036.1:n.-221+795_-221+796del |