Linked Data
MyVariant Identifiers:
chr19:g.7998856G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7933971G>A , CM000681.2:g.7933971G>A | GRCh38 |
| NC_000019.9:g.7998856G>A , CM000681.1:g.7998856G>A | GRCh37 |
| NC_000019.8:g.7904856G>A | NCBI36 |
| NG_051180.1:g.14853C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270538.8:c.576C>T MANE Select | ENSP00000270538.2:p.Asp192= | |
| ENST00000270538.7:c.576C>T | ENSP00000270538.2:p.Asp192= | |
| ENST00000595831.5:c.563C>T | ||
| ENST00000595876.5:c.*264C>T | ENSP00000471596.1:n.*264C>T | |
| ENST00000597926.1:c.480C>T | ENSP00000469389.1:p.Asp160= | |
| ENST00000600748.5:n.561C>T | ||
| NM_006351.3:c.576C>T | NP_006342.2:p.Asp192= | |
| NM_006351.4:c.576C>T MANE Select | NP_006342.2:p.Asp192= |