Linked Data
dbSNP Id:
rs1174549210
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71124128del , CM000664.2:g.71124128del | GRCh38 |
| NC_000002.11:g.71351258del , CM000664.1:g.71351258del | GRCh37 |
| NC_000002.10:g.71204766del | NCBI36 |
| NG_008977.1:g.11138del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000244217.6:c.378+79del MANE Select | ENSP00000244217.5:n.378+79del | |
| ENST00000244217.5:c.378+79del | ENSP00000244217.5:n.378+79del | |
| ENST00000413592.5:c.84+241del | ENSP00000391140.1:n.84+241del | |
| NM_032601.3:c.378+79del | NP_115990.3:n.378+79del | |
| XM_005264613.2:c.216+241del | XP_005264670.1:n.216+241del | |
| XR_939729.1:n.447+79del | ||
| XR_939729.2:n.447+79del | ||
| NM_032601.4:c.378+79del MANE Select | NP_115990.3:n.378+79del |