Linked Data
MyVariant Identifiers:
chr19:g.7998850G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7933965G>T , CM000681.2:g.7933965G>T | GRCh38 |
| NC_000019.9:g.7998850G>T , CM000681.1:g.7998850G>T | GRCh37 |
| NC_000019.8:g.7904850G>T | NCBI36 |
| NG_051180.1:g.14859C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270538.8:c.582C>A MANE Select | ENSP00000270538.2:p.Val194= | |
| ENST00000270538.7:c.582C>A | ENSP00000270538.2:p.Val194= | |
| ENST00000595831.5:c.569C>A | ||
| ENST00000595876.5:c.*270C>A | ENSP00000471596.1:n.*270C>A | |
| ENST00000597926.1:c.486C>A | ENSP00000469389.1:p.Val162= | |
| ENST00000600748.5:n.567C>A | ||
| NM_006351.3:c.582C>A | NP_006342.2:p.Val194= | |
| NM_006351.4:c.582C>A MANE Select | NP_006342.2:p.Val194= |