Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23375785G>A , CM000676.2:g.23375785G>A | GRCh38 |
| NC_000014.8:g.23844994G>A , CM000676.1:g.23844994G>A | GRCh37 |
| NC_000014.7:g.22914834G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397242.3:c.391G>A MANE Select | ENSP00000380417.2:p.Gly131Ser | |
| ENST00000329715.2:c.439G>A | ENSP00000328111.2:p.Gly147Ser | |
| ENST00000397242.2:c.391G>A | ENSP00000380417.2:p.Gly131Ser | |
| NM_022789.3:c.439G>A | NP_073626.1:p.Gly147Ser | |
| NM_172314.1:c.391G>A | NP_758525.1:p.Gly131Ser |