Linked Data
dbSNP Id:
rs945013749
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8733511del , CM000665.2:g.8733511del | GRCh38 |
| NC_000003.11:g.8775197del , CM000665.1:g.8775197del | GRCh37 |
| NC_000003.10:g.8750197del | NCBI36 |
| NG_008797.2:g.4702del , LRG_329:g.4702del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435138.5:c.64+8951del | ENSP00000412333.1:n.64+8951del | |
| ENST00000478513.1:n.335+8951del | ||
| XR_940435.1:n.330+8951del | ||
| XM_017006530.1:c.-283+8951del | XP_016862019.1:n.-283+8951del |