Linked Data
MyVariant Identifiers:
chr19:g.7998787T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7933902T>G , CM000681.2:g.7933902T>G | GRCh38 |
| NC_000019.9:g.7998787T>G , CM000681.1:g.7998787T>G | GRCh37 |
| NC_000019.8:g.7904787T>G | NCBI36 |
| NG_051180.1:g.14922A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270538.8:c.645A>C MANE Select | ENSP00000270538.2:p.Gly215= | |
| ENST00000270538.7:c.645A>C | ENSP00000270538.2:p.Gly215= | |
| ENST00000595831.5:c.632A>C | ||
| ENST00000595876.5:c.*333A>C | ENSP00000471596.1:n.*333A>C | |
| ENST00000597926.1:c.549A>C | ENSP00000469389.1:p.Gly183= | |
| ENST00000598675.1:n.51A>C | ||
| ENST00000600748.5:n.630A>C | ||
| NM_006351.3:c.645A>C | NP_006342.2:p.Gly215= | |
| NM_006351.4:c.645A>C MANE Select | NP_006342.2:p.Gly215= |