Linked Data
dbSNP Id:
rs141985859
gnomAD v2:
1-209806275-TG-T
gnomAD v3:
1-209632930-TG-T
gnomAD v4:
1-209632930-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.209632934del , CM000663.2:g.209632934del | GRCh38 |
| NC_000001.10:g.209806279del , CM000663.1:g.209806279del | GRCh37 |
| NC_000001.9:g.207872902del | NCBI36 |
| NG_007116.1:g.24545del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356082.9:c.628+139del MANE Select | ENSP00000348384.3:n.628+139del | |
| ENST00000356082.8:c.628+139del | ENSP00000348384.3:n.628+139del | |
| ENST00000367030.7:c.628+139del | ENSP00000355997.3:n.628+139del | |
| ENST00000391911.5:c.628+139del | ENSP00000375778.1:n.628+139del | |
| NM_000228.2:c.628+139del | NP_000219.2:n.628+139del | |
| NM_001017402.1:c.628+139del | NP_001017402.1:n.628+139del | |
| NM_001127641.1:c.628+139del | NP_001121113.1:n.628+139del | |
| XM_005273124.3:c.628+139del | XP_005273181.1:n.628+139del | |
| XM_005273124.4:c.628+139del | XP_005273181.1:n.628+139del | |
| XM_017001272.2:c.436+139del | XP_016856761.1:n.436+139del | |
| NM_000228.3:c.628+139del MANE Select | NP_000219.2:n.628+139del | |
| NM_001017402.2:c.628+139del | NP_001017402.1:n.628+139del |