Linked Data
gnomAD v4:
15-58749966-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.58749966G>A , CM000677.2:g.58749966G>A | GRCh38 |
| NC_000015.9:g.59042165G>A , CM000677.1:g.59042165G>A | GRCh37 |
| NC_000015.8:g.56829457G>A | NCBI36 |
| NG_033876.1:g.5013C>T | |
| NG_033876.2:g.4742C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260408.7:c.-432C>T | ENSP00000260408.3:n.-432C>T | |
| NM_001110.3:c.-432C>T | NP_001101.1:n.-432C>T | |
| NM_001320570.1:c.-432C>T | NP_001307499.1:n.-432C>T |