Linked Data
gnomAD v4:
15-65077621-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.65077621G>A , CM000677.2:g.65077621G>A | GRCh38 |
| NC_000015.9:g.65369959G>A , CM000677.1:g.65369959G>A | GRCh37 |
| NC_000015.8:g.63157012G>A | NCBI36 |
| NG_021411.1:g.5806G>A , LRG_682:g.5806G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000432196.5:c.806G>A MANE Select | ENSP00000388723.2:p.Arg269Lys | |
| ENST00000432196.3:c.806G>A | ENSP00000388723.2:p.Arg269Lys | |
| NM_001101362.2:c.806G>A , LRG_682t1:c.806G>A | NP_001094832.1:p.Arg269Lys | |
| NM_001101362.3:c.806G>A MANE Select | NP_001094832.1:p.Arg269Lys |