Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50915839C= , CM000685.2:g.50915839C= | GRCh38 |
| NC_000023.10:g.50658839C= , CM000685.1:g.50658839C= | GRCh37 |
| NC_000023.9:g.50675579C= | NCBI36 |
| NG_012894.1:g.10056C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252677.4:c.411C= MANE Select | ENSP00000252677.3:p.Tyr137= | |
| ENST00000252677.3:c.411C= | ENSP00000252677.3:p.Tyr137= | |
| NM_005448.2:c.411C= MANE Select | NP_005439.2:p.Tyr137= |