Linked Data
dbSNP Id:
rs1564835395
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1018166_1018170delinsGA , CM000673.2:g.1018166_1018170delinsGA | GRCh38 |
| NC_000011.9:g.1018166_1018170delinsGA , CM000673.1:g.1018166_1018170delinsGA | GRCh37 |
| NC_000011.8:g.1008166_1008170delinsGA | NCBI36 |
| NG_052845.1:g.23537_23541delinsTC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000421673.7:c.4631_4635delinsTC MANE Select | ENSP00000406861.2:p.Thr1544del | |
| ENST00000421673.6:c.4631_4635delinsTC | ENSP00000406861.2:p.Thr1544del | |
| NM_005961.2:c.4631_4635delinsTC | NP_005952.2:p.Thr1544del | |
| NM_005961.3:c.4631_4635delinsTC MANE Select | NP_005952.2:p.Thr1544del |