Linked Data
gnomAD v4:
15-44711464-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.44711464C>T , CM000677.2:g.44711464C>T | GRCh38 |
| NC_000015.9:g.45003662C>T , CM000677.1:g.45003662C>T | GRCh37 |
| NC_000015.8:g.42790954C>T | NCBI36 |
| NG_012920.1:g.4978C>T | |
| NG_012920.2:g.4988C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000695792.1:n.83+24C>T |