Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17024065A= , CM000663.2:g.17024065A= | GRCh38 |
| NC_000001.10:g.17350560A= , CM000663.1:g.17350560A= | GRCh37 |
| NC_000001.9:g.17223147A= | NCBI36 |
| NG_012340.1:g.35106T= , LRG_316:g.35106T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.379T= | ENSP00000481376.2:p.Tyr127= | |
| ENST00000491274.6:c.508T= | ENSP00000480482.2:p.Tyr170= | |
| ENST00000375499.8:c.550T= MANE Select | ENSP00000364649.3:p.Tyr184= | |
| ENST00000375499.7:c.550T= | ENSP00000364649.3:p.Tyr184= | |
| ENST00000485515.5:n.484T= | ||
| ENST00000491274.5:c.508T= | ENSP00000480482.1:p.Tyr170= | |
| NM_003000.2:c.550T= , LRG_316t1:c.550T= | NP_002991.2:p.Tyr184= | |
| NM_003000.3:c.550T= MANE Select | NP_002991.2:p.Tyr184= |