Linked Data
dbSNP Id:
rs1585099830
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.16992480del , CM000670.2:g.16992480del | GRCh38 |
| NC_000008.10:g.16849989del , CM000670.1:g.16849989del | GRCh37 |
| NC_000008.9:g.16894360del | NCBI36 |
| NG_015978.1:g.14686del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000180166.6:c.*592del MANE Select | ENSP00000180166.5:n.*592del | |
| ENST00000180166.5:c.*592del | ENSP00000180166.5:n.*592del | |
| NM_019851.3:c.*592del MANE Select | NP_062825.1:n.*592del |