Linked Data
gnomAD v4:
10-102503850-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102503850T>G , CM000672.2:g.102503850T>G | GRCh38 |
| NC_000010.10:g.104263607T>G , CM000672.1:g.104263607T>G | GRCh37 |
| NC_000010.9:g.104253597T>G | NCBI36 |
| NG_011901.1:g.3906A>C | |
| NG_021338.1:g.4889T>G , LRG_521:g.4889T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011539859.1:c.-29-274T>G | XP_011538161.1:n.-29-274T>G | |
| XM_011539863.1:c.8+864T>G | XP_011538165.1:n.8+864T>G | |
| XM_011539863.3:c.8+864T>G | XP_011538165.1:n.8+864T>G |