Linked Data
gnomAD v4:
X-154905062-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154905062A>T , CM000685.2:g.154905062A>T | GRCh38 |
| NC_000023.10:g.154133337A>T , CM000685.1:g.154133337A>T | GRCh37 |
| NC_000023.9:g.153786531A>T | NCBI36 |
| NG_011403.1:g.122662T>A | |
| NG_011403.2:g.122662T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5374-39T>A MANE Select | ENSP00000353393.4:n.5374-39T>A | |
| ENST00000360256.8:c.5374-39T>A | ENSP00000353393.4:n.5374-39T>A | |
| NM_000132.3:c.5374-39T>A | NP_000123.1:n.5374-39T>A | |
| XM_011531126.1:c.5269-39T>A | XP_011529428.1:n.5269-39T>A | |
| NM_000132.4:c.5374-39T>A MANE Select | NP_000123.1:n.5374-39T>A |