Linked Data
dbSNP Id:
rs971147627
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.147413128del , CM000665.2:g.147413128del | GRCh38 |
| NC_000003.11:g.147130915del , CM000665.1:g.147130915del | GRCh37 |
| NC_000003.10:g.148613605del | NCBI36 |
| NG_015886.1:g.8735del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282928.5:c.1147-226del MANE Select | ENSP00000282928.4:n.1147-226del | |
| ENST00000282928.4:c.1147-226del | ENSP00000282928.4:n.1147-226del | |
| ENST00000472523.1:n.521+19186del | ||
| ENST00000488404.5:c.213-226del | ||
| NM_003412.3:c.1147-226del | NP_003403.2:n.1147-226del | |
| NM_003412.4:c.1147-226del MANE Select | NP_003403.2:n.1147-226del |