Linked Data
MyVariant Identifiers:
chr15:g.65370095G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.65077757G>A , CM000677.2:g.65077757G>A | GRCh38 |
| NC_000015.9:g.65370095G>A , CM000677.1:g.65370095G>A | GRCh37 |
| NC_000015.8:g.63157148G>A | NCBI36 |
| NG_021411.1:g.5942G>A , LRG_682:g.5942G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432196.5:c.942G>A MANE Select | ENSP00000388723.2:p.Pro314= | |
| ENST00000432196.3:c.942G>A | ENSP00000388723.2:p.Pro314= | |
| NM_001101362.2:c.942G>A , LRG_682t1:c.942G>A | NP_001094832.1:p.Pro314= | |
| NM_001101362.3:c.942G>A MANE Select | NP_001094832.1:p.Pro314= |