Linked Data
gnomAD v4:
14-74259845-AG-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74259849del , CM000676.2:g.74259849del | GRCh38 |
| NC_000014.8:g.74726552del , CM000676.1:g.74726552del | GRCh37 |
| NC_000014.7:g.73796305del | NCBI36 |
| NG_013092.1:g.25378del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261980.3:c.760+67del MANE Select | ENSP00000261980.2:n.760+67del | |
| ENST00000261980.2:c.760+67del | ENSP00000261980.2:n.760+67del | |
| NM_182894.2:c.760+67del | NP_878314.1:n.760+67del | |
| XM_011536719.1:c.760+67del | XP_011535021.1:n.760+67del | |
| NM_182894.3:c.760+67del MANE Select | NP_878314.1:n.760+67del |