Linked Data
gnomAD v4:
11-6319425-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319425G>A , CM000673.2:g.6319425G>A | GRCh38 |
| NC_000011.9:g.6340655G>A , CM000673.1:g.6340655G>A | GRCh37 |
| NC_000011.8:g.6297231G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.524C>T MANE Select | ENSP00000307292.3:p.Ala175Val | |
| ENST00000303927.3:c.524C>T | ENSP00000307292.3:p.Ala175Val | |
| ENST00000524852.1:n.310C>T | ||
| ENST00000530979.1:c.620C>T | ENSP00000432047.1:p.Ala207Val | |
| ENST00000532354.1:n.546C>T | ||
| NM_145040.2:c.524C>T | NP_659477.2:p.Ala175Val | |
| XR_930997.1:n.720+1205G>A | ||
| XR_001748106.1:n.36G>A | ||
| XR_242848.4:n.285G>A | ||
| NM_145040.3:c.524C>T MANE Select | NP_659477.2:p.Ala175Val |