Linked Data
gnomAD v4:
15-65077599-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.65077599G>T , CM000677.2:g.65077599G>T | GRCh38 |
| NC_000015.9:g.65369937G>T , CM000677.1:g.65369937G>T | GRCh37 |
| NC_000015.8:g.63156990G>T | NCBI36 |
| NG_021411.1:g.5784G>T , LRG_682:g.5784G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432196.5:c.784G>T MANE Select | ENSP00000388723.2:p.Ala262Ser | |
| ENST00000432196.3:c.784G>T | ENSP00000388723.2:p.Ala262Ser | |
| NM_001101362.2:c.784G>T , LRG_682t1:c.784G>T | NP_001094832.1:p.Ala262Ser | |
| NM_001101362.3:c.784G>T MANE Select | NP_001094832.1:p.Ala262Ser |