Linked Data
gnomAD v4:
21-44456980-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44456985del , CM000683.2:g.44456985del | GRCh38 |
| NC_000021.8:g.45876868del , CM000683.1:g.45876868del | GRCh37 |
| NC_000021.7:g.44701296del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291592.6:c.341del MANE Select | ENSP00000291592.4:p.Gly114AlafsTer? | |
| ENST00000291592.5:c.341del | ENSP00000291592.4:p.Gly114AlafsTer? | |
| NM_030891.4:c.341del | NP_112153.1:p.Gly114AlafsTer? | |
| NM_030891.5:c.341del | NP_112153.1:p.Gly114AlafsTer? | |
| NM_030891.6:c.341del MANE Select | NP_112153.1:p.Gly114AlafsTer? |