Linked Data
dbSNP Id:
rs1568555759
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18787868_18787873dup , CM000681.2:g.18787868_18787873dup | GRCh38 |
| NC_000019.9:g.18898677_18898682dup , CM000681.1:g.18898677_18898682dup | GRCh37 |
| NC_000019.8:g.18759677_18759682dup | NCBI36 |
| NG_007070.1:g.8434_8439dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.976-222_976-217dup MANE Select | ENSP00000222271.2:n.976-222_976-217dup | |
| ENST00000222271.6:c.976-222_976-217dup | ENSP00000222271.2:n.976-222_976-217dup | |
| ENST00000425807.1:c.817-222_817-217dup | ENSP00000403792.1:n.817-222_817-217dup | |
| ENST00000542601.6:c.877-222_877-217dup | ENSP00000439156.2:n.877-222_877-217dup | |
| NM_000095.2:c.976-222_976-217dup | NP_000086.2:n.976-222_976-217dup | |
| NM_000095.3:c.976-222_976-217dup MANE Select | NP_000086.2:n.976-222_976-217dup |