Linked Data
dbSNP Id:
rs1402091457
gnomAD v2:
1-68896943-AT-A
gnomAD v3:
1-68431260-AT-A
gnomAD v4:
1-68431260-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68431262del , CM000663.2:g.68431262del | GRCh38 |
| NC_000001.10:g.68896945del , CM000663.1:g.68896945del | GRCh37 |
| NC_000001.9:g.68669533del | NCBI36 |
| NG_008472.1:g.23699del | |
| NG_008472.2:g.23699del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1338+21del MANE Select | ENSP00000262340.5:n.1338+21del | |
| ENST00000262340.5:c.1338+21del | ENSP00000262340.5:n.1338+21del | |
| NM_000329.2:c.1338+21del | NP_000320.1:n.1338+21del | |
| XM_017002027.1:c.1062+21del | XP_016857516.1:n.1062+21del | |
| NM_000329.3:c.1338+21del MANE Select | NP_000320.1:n.1338+21del |