Linked Data
gnomAD v4:
12-5044267-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5044270del , CM000674.2:g.5044270del | GRCh38 |
| NC_000012.11:g.5153436del , CM000674.1:g.5153436del | GRCh37 |
| NC_000012.10:g.5023697del | NCBI36 |
| NG_012198.1:g.5352del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.123del MANE Select | ENSP00000252321.3:p.Leu42SerfsTer? | |
| ENST00000252321.4:c.123del | ENSP00000252321.3:p.Leu42SerfsTer? | |
| NM_002234.3:c.123del | NP_002225.2:p.Leu42SerfsTer? | |
| NM_002234.4:c.123del MANE Select | NP_002225.2:p.Leu42SerfsTer? |