Linked Data
gnomAD v4:
15-44711461-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.44711461T>C , CM000677.2:g.44711461T>C | GRCh38 |
| NC_000015.9:g.45003659T>C , CM000677.1:g.45003659T>C | GRCh37 |
| NC_000015.8:g.42790951T>C | NCBI36 |
| NG_012920.1:g.4975T>C | |
| NG_012920.2:g.4985T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695792.1:n.83+21T>C |