Linked Data
gnomAD v4:
4-24800029-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24800029C>A , CM000666.2:g.24800029C>A | GRCh38 |
| NC_000004.11:g.24801651C>A , CM000666.1:g.24801651C>A | GRCh37 |
| NC_000004.10:g.24410749C>A | NCBI36 |
| NG_012213.1:g.9567C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.508C>A MANE Select | ENSP00000371554.3:p.Pro170Thr | |
| ENST00000382120.3:c.508C>A | ENSP00000371554.3:p.Pro170Thr | |
| NM_003102.2:c.508C>A | NP_003093.2:p.Pro170Thr | |
| XR_427488.1:n.698C>A | ||
| NM_003102.3:c.508C>A | NP_003093.2:p.Pro170Thr | |
| NM_003102.4:c.508C>A MANE Select | NP_003093.2:p.Pro170Thr |