Linked Data
gnomAD v4:
20-31820215-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.31820215C>A , CM000682.2:g.31820215C>A | GRCh38 |
| NC_000020.10:g.30408018C>A , CM000682.1:g.30408018C>A | GRCh37 |
| NC_000020.9:g.29871679C>A | NCBI36 |
| NG_012847.1:g.5841C>A , LRG_392:g.5841C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375985.5:c.142C>A MANE Select | ENSP00000365152.4:p.Pro48Thr | |
| ENST00000375985.4:c.142C>A | ENSP00000365152.4:p.Pro48Thr | |
| ENST00000375994.6:c.142C>A | ENSP00000365162.2:p.Pro48Thr | |
| NM_033118.3:c.142C>A , LRG_392t1:c.142C>A | NP_149109.1:p.Pro48Thr | |
| XR_244155.1:n.307C>A | ||
| NM_033118.4:c.142C>A MANE Select | NP_149109.1:p.Pro48Thr |