Linked Data
gnomAD v4:
21-31667380-GT-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31667384del , CM000683.2:g.31667384del | GRCh38 |
| NC_000021.8:g.33039697del , CM000683.1:g.33039697del | GRCh37 |
| NC_000021.7:g.31961568del | NCBI36 |
| NG_008689.1:g.12763del , LRG_652:g.12763del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270142.11:c.357+9del MANE Select | ENSP00000270142.7:n.357+9del | |
| ENST00000270142.10:c.357+9del | ENSP00000270142.6:n.357+9del | |
| ENST00000389995.4:c.300+9del | ENSP00000374645.4:n.300+9del | |
| ENST00000470944.1:n.1285+9del | ||
| NM_000454.4:c.357+9del , LRG_652t1:c.357+9del | NP_000445.1:n.357+9del | |
| NM_000454.5:c.357+9del MANE Select | NP_000445.1:n.357+9del |