Linked Data
MyVariant Identifiers:
chr7:g.107315551_107315555del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107675106_107675110del , CM000669.2:g.107675106_107675110del | GRCh38 |
| NC_000007.13:g.107315551_107315555del , CM000669.1:g.107315551_107315555del | GRCh37 |
| NC_000007.12:g.107102787_107102791del | NCBI36 |
| NG_008489.1:g.19472_19476del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.762_765+1del | ||
| ENST00000265715.7:c.762_765+1del | ||
| NM_000441.1:c.762_765+1del | ||
| XM_005250425.1:c.762_765+1del | ||
| XM_006716025.2:c.762_765+1del | ||
| XM_005250425.2:c.762_765+1del | ||
| XM_006716025.3:c.762_765+1del | ||
| XM_017012318.1:c.762_765+1del | ||
| NM_000441.2:c.762_765+1del |