Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075692A>T , CM000679.2:g.8075692A>T | GRCh38 |
| NC_000017.10:g.7979010A>T , CM000679.1:g.7979010A>T | GRCh37 |
| NC_000017.9:g.7919735A>T | NCBI36 |
| NG_007099.1:g.17012T>A | |
| NG_007099.2:g.17025T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647874.1:c.1557T>A MANE Select | ENSP00000497784.1:p.Tyr519Ter | |
| ENST00000649809.1:c.621T>A | ENSP00000496845.1:p.Tyr207Ter | |
| ENST00000319144.4:c.1557T>A | ENSP00000315167.4:p.Tyr519Ter | |
| ENST00000577351.5:n.479+483T>A | ||
| NM_001139.2:c.1557T>A | NP_001130.1:p.Tyr519Ter | |
| NM_001139.3:c.1557T>A MANE Select | NP_001130.1:p.Tyr519Ter |