Linked Data
gnomAD v4:
1-114684363-ACCTG-A
MyVariant Identifiers:
chr1:g.115226985_115226988del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114684366_114684369del , CM000663.2:g.114684366_114684369del | GRCh38 |
| NC_000001.10:g.115226987_115226990del , CM000663.1:g.115226987_115226990del | GRCh37 |
| NC_000001.9:g.115028510_115028513del | NCBI36 |
| NG_008012.1:g.16189_16192del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369538.4:c.370-3_370del | ||
| ENST00000520113.7:c.382-3_382del | ||
| ENST00000637080.1:c.385-3_385del | ||
| ENST00000639077.1:n.47-3_47del | ||
| ENST00000369538.3:c.469-3_469del | ||
| ENST00000485564.3:n.256-3_256del | ||
| ENST00000520113.6:c.481-3_481del | ||
| NM_000036.2:c.481-3_481del | ||
| NM_001172626.1:c.469-3_469del | ||
| NM_000036.3:c.382-3_382del | ||
| NM_001172626.2:c.370-3_370del |