Linked Data
gnomAD v4:
12-57764562-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57764562G>T , CM000674.2:g.57764562G>T | GRCh38 |
| NC_000012.11:g.58158345G>T , CM000674.1:g.58158345G>T | GRCh37 |
| NC_000012.10:g.56444612G>T | NCBI36 |
| NG_007076.1:g.7632C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713544.1:c.1045-12C>A | ENSP00000518840.1:n.1045-12C>A | |
| ENST00000713545.1:c.1022-12C>A | ENSP00000518841.1:n.1022-12C>A | |
| ENST00000228606.9:c.964-12C>A MANE Select | ENSP00000228606.4:n.964-12C>A | |
| ENST00000228606.8:c.964-12C>A | ENSP00000228606.4:n.964-12C>A | |
| ENST00000546567.5:c.259-12C>A | ENSP00000449472.1:n.259-12C>A | |
| ENST00000547344.5:n.1103-12C>A | ||
| ENST00000547451.1:n.955C>A | ||
| NM_000785.3:c.964-12C>A | NP_000776.1:n.964-12C>A | |
| NM_000785.4:c.964-12C>A MANE Select | NP_000776.1:n.964-12C>A |