Linked Data
gnomAD v4:
12-57763610-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57763610C>A , CM000674.2:g.57763610C>A | GRCh38 |
| NC_000012.11:g.58157393C>A , CM000674.1:g.58157393C>A | GRCh37 |
| NC_000012.10:g.56443660C>A | NCBI36 |
| NG_007076.1:g.8584G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713544.1:c.1494+1G>T | ENSP00000518840.1:n.1494+1G>T | |
| ENST00000713545.1:c.*418+1G>T | ENSP00000518841.1:n.*418+1G>T | |
| ENST00000228606.9:c.1413+1G>T MANE Select | ENSP00000228606.4:n.1413+1G>T | |
| ENST00000228606.8:c.1413+1G>T | ENSP00000228606.4:n.1413+1G>T | |
| ENST00000547344.5:n.1552+1G>T | ||
| NM_000785.3:c.1413+1G>T | NP_000776.1:n.1413+1G>T | |
| NM_000785.4:c.1413+1G>T MANE Select | NP_000776.1:n.1413+1G>T |