Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128845111T= , CM000669.2:g.128845111T= | GRCh38 |
| NC_000007.13:g.128485165T= , CM000669.1:g.128485165T= | GRCh37 |
| NC_000007.12:g.128272401T= | NCBI36 |
| NG_011807.1:g.19683T= , LRG_870:g.19683T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.3646T= MANE Select | ENSP00000327145.8:p.Tyr1216= | |
| ENST00000325888.12:c.3646T= | ENSP00000327145.8:p.Tyr1216= | |
| ENST00000346177.6:c.3646T= | ENSP00000344002.6:p.Tyr1216= | |
| NM_001127487.1:c.3646T= | NP_001120959.1:p.Tyr1216= | |
| NM_001458.4:c.3646T= , LRG_870t1:c.3646T= | NP_001449.3:p.Tyr1216= | |
| NM_001127487.2:c.3646T= | NP_001120959.1:p.Tyr1216= | |
| NM_001458.5:c.3646T= MANE Select | NP_001449.3:p.Tyr1216= |