Linked Data
gnomAD v4:
6-49451607-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.49451609del , CM000668.2:g.49451609del | GRCh38 |
| NC_000006.11:g.49419322del , CM000668.1:g.49419322del | GRCh37 |
| NC_000006.10:g.49527281del | NCBI36 |
| NG_007100.1:g.16532del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274813.4:c.1190del MANE Select | ENSP00000274813.3:p.Pro397GlnfsTer3 | |
| ENST00000274813.3:c.1190del | ENSP00000274813.3:p.Pro397GlnfsTer3 | |
| NM_000255.3:c.1190del | NP_000246.2:p.Pro397GlnfsTer3 | |
| XM_005249143.2:c.1190del | XP_005249200.1:p.Pro397GlnfsTer3 | |
| XM_005249143.3:c.1190del | XP_005249200.1:p.Pro397GlnfsTer3 | |
| NM_000255.4:c.1190del MANE Select | NP_000246.2:p.Pro397GlnfsTer3 |