Linked Data
gnomAD v4:
15-58749910-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.58749910C>A , CM000677.2:g.58749910C>A | GRCh38 |
| NC_000015.9:g.59042109C>A , CM000677.1:g.59042109C>A | GRCh37 |
| NC_000015.8:g.56829401C>A | NCBI36 |
| NG_033876.1:g.5069G>T | |
| NG_033876.2:g.4798G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260408.7:c.-376G>T | ENSP00000260408.3:n.-376G>T | |
| NM_001110.3:c.-376G>T | NP_001101.1:n.-376G>T | |
| NM_001320570.1:c.-376G>T | NP_001307499.1:n.-376G>T |