Linked Data
gnomAD v4:
X-119930222-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.119930224del , CM000685.2:g.119930224del | GRCh38 |
| NC_000023.10:g.119064187del , CM000685.1:g.119064187del | GRCh37 |
| NC_000023.9:g.118948215del | NCBI36 |
| NG_021260.1:g.18550del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371410.5:c.924-58del MANE Select | ENSP00000360464.3:n.924-58del | |
| ENST00000652253.1:c.920-58del | ||
| ENST00000371410.4:c.924-58del | ENSP00000360464.3:n.924-58del | |
| ENST00000477789.5:n.1852-58del | ||
| ENST00000482407.1:n.723-58del | ||
| NM_024528.3:c.924-58del | NP_078804.2:n.924-58del | |
| XM_017029842.1:c.627-58del | XP_016885331.1:n.627-58del | |
| NM_024528.4:c.924-58del MANE Select | NP_078804.2:n.924-58del |