Linked Data
gnomAD v4:
6-49457674-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.49457675del , CM000668.2:g.49457675del | GRCh38 |
| NC_000006.11:g.49425388del , CM000668.1:g.49425388del | GRCh37 |
| NC_000006.10:g.49533347del | NCBI36 |
| NG_007100.1:g.10465del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274813.4:c.753+16del MANE Select | ENSP00000274813.3:n.753+16del | |
| ENST00000274813.3:c.753+16del | ENSP00000274813.3:n.753+16del | |
| NM_000255.3:c.753+16del | NP_000246.2:n.753+16del | |
| XM_005249143.2:c.753+16del | XP_005249200.1:n.753+16del | |
| XM_005249143.3:c.753+16del | XP_005249200.1:n.753+16del | |
| NM_000255.4:c.753+16del MANE Select | NP_000246.2:n.753+16del |