Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22625359T= , CM000673.2:g.22625359T= | GRCh38 |
| NC_000011.9:g.22646905T= , CM000673.1:g.22646905T= | GRCh37 |
| NC_000011.8:g.22603481T= | NCBI36 |
| NG_007425.1:g.5483A= , LRG_527:g.5483A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327470.6:c.452A= MANE Select | ENSP00000330875.3:p.Tyr151= | |
| ENST00000327470.4:c.452A= | ENSP00000330875.3:p.Tyr151= | |
| NM_022725.3:c.452A= , LRG_527t1:c.452A= | NP_073562.1:p.Tyr151= | |
| NM_022725.4:c.452A= MANE Select | NP_073562.1:p.Tyr151= |