Linked Data
gnomAD v4:
5-148827152-GT-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.148827156del , CM000667.2:g.148827156del | GRCh38 |
| NC_000005.9:g.148206719del , CM000667.1:g.148206719del | GRCh37 |
| NC_000005.8:g.148186912del | NCBI36 |
| NG_016421.1:g.5564del | |
| NG_016421.2:g.5564del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305988.6:c.325del MANE Select | ENSP00000305372.4:p.Trp109GlyfsTer18 | |
| ENST00000305988.5:c.325del | ENSP00000305372.4:p.Trp109GlyfsTer18 | |
| NM_000024.5:c.325del | NP_000015.1:p.Trp109GlyfsTer18 | |
| NM_000024.6:c.325del MANE Select | NP_000015.2:p.Trp109GlyfsTer18 |