Linked Data
dbSNP Id:
rs1463865814
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19966947_19966953del , CM000670.2:g.19966947_19966953del | GRCh38 |
| NC_000008.10:g.19824458_19824464del , CM000670.1:g.19824458_19824464del | GRCh37 |
| NC_000008.9:g.19868738_19868744del | NCBI36 |
| NG_008855.1:g.32877_32883del | |
| NG_008855.2:g.70231_70237del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650287.1:c.*1637_*1643del MANE Select | ENSP00000497642.1:n.*1637_*1643del | |
| ENST00000650478.1:c.2005_2011del | ENSP00000497560.1:n.2005_2011del | |
| ENST00000311322.8:c.*1637_*1643del | ENSP00000309757.6:n.*1637_*1643del | |
| NM_000237.2:c.*1637_*1643del | NP_000228.1:n.*1637_*1643del | |
| NM_000237.3:c.*1637_*1643del MANE Select | NP_000228.1:n.*1637_*1643del |