Linked Data
gnomAD v4:
1-149925806-TCCCTC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149925809_149925813del , CM000663.2:g.149925809_149925813del | GRCh38 |
| NC_000001.10:g.149897701_149897705del , CM000663.1:g.149897701_149897705del | GRCh37 |
| NC_000001.9:g.148164325_148164329del | NCBI36 |
| NG_032777.1:g.7442_7446del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.9:c.913+25_913+29del MANE Select | ENSP00000271628.8:n.913+25_913+29del | |
| ENST00000271628.8:c.913+25_913+29del | ENSP00000271628.8:n.913+25_913+29del | |
| NM_005850.4:c.913+25_913+29del | NP_005841.1:n.913+25_913+29del | |
| NM_005850.5:c.913+25_913+29del MANE Select | NP_005841.1:n.913+25_913+29del |