Linked Data
gnomAD v4:
17-4631228-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4631228T>A , CM000679.2:g.4631228T>A | GRCh38 |
| NC_000017.10:g.4534523T>A , CM000679.1:g.4534523T>A | GRCh37 |
| NC_000017.9:g.4481272T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293761.8:c.*372A>T MANE Select | ENSP00000293761.3:n.*372A>T | |
| ENST00000293761.7:c.*372A>T | ENSP00000293761.3:n.*372A>T | |
| ENST00000570836.5:c.*372A>T | ENSP00000458832.1:n.*372A>T | |
| NM_001140.3:c.*372A>T | NP_001131.3:n.*372A>T | |
| NM_001140.4:c.*372A>T | NP_001131.3:n.*372A>T | |
| NM_001140.5:c.*372A>T MANE Select | NP_001131.3:n.*372A>T |