Linked Data
gnomAD v4:
15-65029582-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.65029582G>T , CM000677.2:g.65029582G>T | GRCh38 |
| NC_000015.9:g.65321920G>T , CM000677.1:g.65321920G>T | GRCh37 |
| NC_000015.8:g.63108973G>T | NCBI36 |
| NG_029184.1:g.5058C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000220058.9:c.32C>A MANE Select | ENSP00000220058.4:p.Pro11His | |
| ENST00000220058.8:c.32C>A | ENSP00000220058.4:p.Pro11His | |
| ENST00000543678.1:c.32C>A | ENSP00000443754.1:p.Pro11His | |
| ENST00000558460.5:c.32C>A | ENSP00000452646.1:p.Pro11His | |
| ENST00000560717.5:c.17C>A | ENSP00000457257.1:p.Pro6His | |
| NM_139242.3:c.32C>A | NP_640335.2:p.Pro11His | |
| XM_005254158.5:c.32C>A | XP_005254215.2:p.Pro11His | |
| XR_001751081.1:n.47C>A | ||
| NM_139242.4:c.32C>A MANE Select | NP_640335.2:p.Pro11His |