Linked Data
gnomAD v4:
10-43077038-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.43077038C>A , CM000672.2:g.43077038C>A | GRCh38 |
| NC_000010.10:g.43572486C>A , CM000672.1:g.43572486C>A | GRCh37 |
| NC_000010.9:g.42892492C>A | NCBI36 |
| NG_007489.1:g.4970C>A , LRG_518:g.4970C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355710.7:c.-221C>A | ENSP00000347942.3:n.-221C>A | |
| XM_011540027.1:c.-221C>A | XP_011538329.1:n.-221C>A | |
| NM_020630.5:c.-221C>A | NP_065681.1:n.-221C>A | |
| NM_020975.5:c.-221C>A | NP_066124.1:n.-221C>A |