Linked Data
gnomAD v4:
X-25004487-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25004487A>T , CM000685.2:g.25004487A>T | GRCh38 |
| NC_000023.10:g.25022604A>T , CM000685.1:g.25022604A>T | GRCh37 |
| NC_000023.9:g.24932525A>T | NCBI36 |
| NG_008281.1:g.16462T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.*183T>A MANE Select | ENSP00000368332.4:n.*183T>A | |
| ENST00000379044.4:c.*183T>A | ENSP00000368332.4:n.*183T>A | |
| NM_139058.2:c.*183T>A | NP_620689.1:n.*183T>A | |
| NM_139058.3:c.*183T>A MANE Select | NP_620689.1:n.*183T>A |