Linked Data
dbSNP Id:
rs1568968688
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.27750496del , CM000684.2:g.27750496del | GRCh38 |
| NC_000022.10:g.28146484del , CM000684.1:g.28146484del | GRCh37 |
| NC_000022.9:g.26476484del | NCBI36 |
| NG_023258.1:g.56008del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703102.1:n.912del | ||
| ENST00000302326.5:c.*424del MANE Select | ENSP00000304956.4:n.*424del | |
| ENST00000302326.4:c.*424del | ENSP00000304956.4:n.*424del | |
| ENST00000424656.1:c.456-263del | ||
| NM_002430.2:c.*424del | NP_002421.3:n.*424del | |
| NM_002430.3:c.*424del MANE Select | NP_002421.3:n.*424del |