Linked Data
gnomAD v4:
1-43337825-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.43337825G>A , CM000663.2:g.43337825G>A | GRCh38 |
| NC_000001.10:g.43803496G>A , CM000663.1:g.43803496G>A | GRCh37 |
| NC_000001.9:g.43576083G>A | NCBI36 |
| NG_007525.1:g.5022G>A , LRG_510:g.5022G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372470.9:c.-24G>A MANE Select | ENSP00000361548.3:n.-24G>A | |
| ENST00000372470.7:c.-24G>A | ENSP00000361548.3:n.-24G>A | |
| NM_005373.2:c.-24G>A , LRG_510t1:c.-24G>A | NP_005364.1:n.-24G>A | |
| XM_011541478.1:c.-24G>A | XP_011539780.1:n.-24G>A | |
| XM_017001320.1:c.-24G>A | XP_016856809.1:n.-24G>A | |
| NM_005373.3:c.-24G>A MANE Select | NP_005364.1:n.-24G>A |