Linked Data
gnomAD v4:
12-21174510-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21174514del , CM000674.2:g.21174514del | GRCh38 |
| NC_000012.11:g.21327448del , CM000674.1:g.21327448del | GRCh37 |
| NC_000012.10:g.21218715del | NCBI36 |
| NG_011745.1:g.48321del , LRG_1022:g.48321del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.227-63del MANE Select | ENSP00000256958.2:n.227-63del | |
| ENST00000256958.2:c.227-63del | ENSP00000256958.2:n.227-63del | |
| ENST00000543498.5:c.426-2262del | ||
| NM_006446.4:c.227-63del , LRG_1022t1:c.227-63del | NP_006437.3:n.227-63del | |
| NM_006446.5:c.227-63del MANE Select | NP_006437.3:n.227-63del |