Linked Data
gnomAD v4:
12-52433745-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52433745A>T , CM000674.2:g.52433745A>T | GRCh38 |
| NC_000012.11:g.52827529A>T , CM000674.1:g.52827529A>T | GRCh37 |
| NC_000012.10:g.51113796A>T | NCBI36 |
| NG_008403.1:g.5582T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252245.6:c.498+62T>A MANE Select | ENSP00000252245.5:n.498+62T>A | |
| ENST00000252245.5:c.498+62T>A | ENSP00000252245.5:n.498+62T>A | |
| NM_004693.2:c.498+62T>A | NP_004684.2:n.498+62T>A | |
| NM_004693.3:c.498+62T>A MANE Select | NP_004684.2:n.498+62T>A |