Linked Data
dbSNP Id:
rs1756519212
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1423834del , CM000667.2:g.1423834del | GRCh38 |
| NC_000005.9:g.1423949del , CM000667.1:g.1423949del | GRCh37 |
| NC_000005.8:g.1476949del | NCBI36 |
| NG_015885.1:g.26595del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.654-1820del MANE Select | ENSP00000270349.9:n.654-1820del | |
| ENST00000270349.11:c.654-1820del | ENSP00000270349.9:n.654-1820del | |
| NM_001044.4:c.654-1820del | NP_001035.1:n.654-1820del | |
| NM_001044.5:c.654-1820del MANE Select | NP_001035.1:n.654-1820del |