Linked Data
gnomAD v4:
15-65077569-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.65077569G>A , CM000677.2:g.65077569G>A | GRCh38 |
| NC_000015.9:g.65369907G>A , CM000677.1:g.65369907G>A | GRCh37 |
| NC_000015.8:g.63156960G>A | NCBI36 |
| NG_021411.1:g.5754G>A , LRG_682:g.5754G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432196.5:c.754G>A MANE Select | ENSP00000388723.2:p.Ala252Thr | |
| ENST00000432196.3:c.754G>A | ENSP00000388723.2:p.Ala252Thr | |
| NM_001101362.2:c.754G>A , LRG_682t1:c.754G>A | NP_001094832.1:p.Ala252Thr | |
| NM_001101362.3:c.754G>A MANE Select | NP_001094832.1:p.Ala252Thr |