Linked Data
dbSNP Id:
rs2075076020
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17381874del , CM000663.2:g.17381874del | GRCh38 |
| NC_000001.10:g.17708369del , CM000663.1:g.17708369del | GRCh37 |
| NC_000001.9:g.17580956del | NCBI36 |
| NG_032943.1:g.14629del | |
| NG_032943.2:g.14629del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619609.1:c.554-93del MANE Select | ENSP00000483125.1:n.554-93del | |
| NM_207421.4:c.554-93del MANE Select | NP_997304.3:n.554-93del |