Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075692A>G , CM000679.2:g.8075692A>G | GRCh38 |
| NC_000017.10:g.7979010A>G , CM000679.1:g.7979010A>G | GRCh37 |
| NC_000017.9:g.7919735A>G | NCBI36 |
| NG_007099.1:g.17012T>C | |
| NG_007099.2:g.17025T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647874.1:c.1557T>C MANE Select | ENSP00000497784.1:p.Tyr519= | |
| ENST00000649809.1:c.621T>C | ENSP00000496845.1:p.Tyr207= | |
| ENST00000319144.4:c.1557T>C | ENSP00000315167.4:p.Tyr519= | |
| ENST00000577351.5:n.479+483T>C | ||
| NM_001139.2:c.1557T>C | NP_001130.1:p.Tyr519= | |
| NM_001139.3:c.1557T>C MANE Select | NP_001130.1:p.Tyr519= |