Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24800067T= , CM000666.2:g.24800067T= | GRCh38 |
| NC_000004.11:g.24801689T= , CM000666.1:g.24801689T= | GRCh37 |
| NC_000004.10:g.24410787T= | NCBI36 |
| NG_012213.1:g.9605T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.546T= MANE Select | ENSP00000371554.3:p.Ala182= | |
| ENST00000382120.3:c.546T= | ENSP00000371554.3:p.Ala182= | |
| NM_003102.2:c.546T= | NP_003093.2:p.Ala182= | |
| XR_427488.1:n.736T= | ||
| NM_003102.3:c.546T= | NP_003093.2:p.Ala182= | |
| NM_003102.4:c.546T= MANE Select | NP_003093.2:p.Ala182= |