Linked Data
gnomAD v4:
10-122506692-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122506692G>A , CM000672.2:g.122506692G>A | GRCh38 |
| NC_000010.10:g.124266208G>A , CM000672.1:g.124266208G>A | GRCh37 |
| NC_000010.9:g.124256198G>A | NCBI36 |
| NG_011554.1:g.50168G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.779G>A MANE Select | ENSP00000357980.3:p.Gly260Asp | |
| ENST00000648167.1:c.461G>A | ENSP00000498033.1:p.Gly154Asp | |
| ENST00000368984.7:c.779G>A | ENSP00000357980.3:p.Gly260Asp | |
| ENST00000420892.1:c.2G>A | ENSP00000412676.1:p.Gly1Asp | |
| NM_002775.4:c.779G>A | NP_002766.1:p.Gly260Asp | |
| NM_002775.5:c.779G>A MANE Select | NP_002766.1:p.Gly260Asp |