Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74750200T= , CM000677.2:g.74750200T= | GRCh38 |
| NC_000015.9:g.75042541T= , CM000677.1:g.75042541T= | GRCh37 |
| NC_000015.8:g.72829594T= | NCBI36 |
| NG_008431.1:g.32659T= | |
| NG_008431.2:g.32659T= | |
| NG_061543.1:g.6356T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.462T= MANE Select | ENSP00000342007.4:p.Ala154= | |
| ENST00000343932.4:c.462T= | ENSP00000342007.4:p.Ala154= | |
| NM_000761.4:c.462T= | NP_000752.2:p.Ala154= | |
| NM_000761.5:c.462T= MANE Select | NP_000752.2:p.Ala154= |