Linked Data
gnomAD v4:
10-94942628-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94942628T>A , CM000672.2:g.94942628T>A | GRCh38 |
| NC_000010.10:g.96702385T>A , CM000672.1:g.96702385T>A | GRCh37 |
| NC_000010.9:g.96692375T>A | NCBI36 |
| NG_008385.1:g.8971T>A | |
| NG_008385.2:g.9471T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.481+287T>A MANE Select | ENSP00000260682.6:n.481+287T>A | |
| ENST00000643112.1:c.481+287T>A | ENSP00000496202.1:n.481+287T>A | |
| ENST00000645207.1:n.634+287T>A | ||
| ENST00000260682.6:c.481+287T>A | ENSP00000260682.6:n.481+287T>A | |
| ENST00000461906.1:n.793T>A | ||
| ENST00000473496.1:n.252+287T>A | ||
| NM_000771.3:c.481+287T>A | NP_000762.2:n.481+287T>A | |
| NM_000771.4:c.481+287T>A MANE Select | NP_000762.2:n.481+287T>A |