Linked Data
gnomAD v4:
10-102503938-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102503938C>A , CM000672.2:g.102503938C>A | GRCh38 |
| NC_000010.10:g.104263695C>A , CM000672.1:g.104263695C>A | GRCh37 |
| NC_000010.9:g.104253685C>A | NCBI36 |
| NG_011901.1:g.3818G>T | |
| NG_021338.1:g.4977C>A , LRG_521:g.4977C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011539859.1:c.-29-186C>A | XP_011538161.1:n.-29-186C>A | |
| XM_011539863.1:c.8+952C>A | XP_011538165.1:n.8+952C>A | |
| XM_011539863.3:c.8+952C>A | XP_011538165.1:n.8+952C>A |