Linked Data
gnomAD v4:
X-50910756-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50910756C>A , CM000685.2:g.50910756C>A | GRCh38 |
| NC_000023.10:g.50653756C>A , CM000685.1:g.50653756C>A | GRCh37 |
| NC_000023.9:g.50670496C>A | NCBI36 |
| NG_012894.1:g.4973C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252677.4:c.-28C>A MANE Select | ENSP00000252677.3:n.-28C>A | |
| NM_005448.2:c.-28C>A MANE Select | NP_005439.2:n.-28C>A |