Linked Data
gnomAD v4:
7-21748546-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21748550del , CM000669.2:g.21748550del | GRCh38 |
| NC_000007.13:g.21788168del , CM000669.1:g.21788168del | GRCh37 |
| NC_000007.12:g.21754693del | NCBI36 |
| NG_012886.2:g.210336del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.8511-30del MANE Select | ENSP00000475939.1:n.8511-30del | |
| ENST00000328843.10:c.8532-30del | ENSP00000330671.7:n.8532-30del | |
| ENST00000409508.7:c.8511-30del | ENSP00000475939.1:n.8511-30del | |
| ENST00000620169.4:c.8532-30del | ENSP00000481693.1:n.8532-30del | |
| NM_001277115.1:c.8511-30del | NP_001264044.1:n.8511-30del | |
| NM_001277115.2:c.8511-30del MANE Select | NP_001264044.1:n.8511-30del |