Linked Data
gnomAD v4:
10-102503863-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102503863C>A , CM000672.2:g.102503863C>A | GRCh38 |
| NC_000010.10:g.104263620C>A , CM000672.1:g.104263620C>A | GRCh37 |
| NC_000010.9:g.104253610C>A | NCBI36 |
| NG_011901.1:g.3893G>T | |
| NG_021338.1:g.4902C>A , LRG_521:g.4902C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011539859.1:c.-29-261C>A | XP_011538161.1:n.-29-261C>A | |
| XM_011539863.1:c.8+877C>A | XP_011538165.1:n.8+877C>A | |
| XM_011539863.3:c.8+877C>A | XP_011538165.1:n.8+877C>A |