Linked Data
gnomAD v4:
10-94989050-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94989050G>A , CM000672.2:g.94989050G>A | GRCh38 |
| NC_000010.10:g.96748807G>A , CM000672.1:g.96748807G>A | GRCh37 |
| NC_000010.9:g.96738797G>A | NCBI36 |
| NG_008385.1:g.55393G>A | |
| NG_008385.2:g.55893G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.*22G>A MANE Select | ENSP00000260682.6:n.*22G>A | |
| ENST00000643112.1:c.*504G>A | ENSP00000496202.1:n.*504G>A | |
| ENST00000260682.6:c.*22G>A | ENSP00000260682.6:n.*22G>A | |
| NM_000771.3:c.*22G>A | NP_000762.2:n.*22G>A | |
| NM_000771.4:c.*22G>A MANE Select | NP_000762.2:n.*22G>A |