Linked Data
gnomAD v4:
14-75135058-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75135058G>T , CM000676.2:g.75135058G>T | GRCh38 |
| NC_000014.8:g.75601761G>T , CM000676.1:g.75601761G>T | GRCh37 |
| NC_000014.7:g.74671514G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303575.9:c.539-52C>A MANE Select | ENSP00000303145.4:n.539-52C>A | |
| ENST00000303575.8:c.539-52C>A | ENSP00000303145.4:n.539-52C>A | |
| ENST00000555036.1:n.322-52C>A | ||
| ENST00000555873.1:c.*175-52C>A | ENSP00000450726.1:n.*175-52C>A | |
| ENST00000556969.5:n.246-52C>A | ||
| ENST00000557670.5:n.267-52C>A | ||
| NM_006827.5:c.539-52C>A | NP_006818.3:n.539-52C>A | |
| NM_006827.6:c.539-52C>A MANE Select | NP_006818.3:n.539-52C>A |