Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24800249G= , CM000666.2:g.24800249G= | GRCh38 |
| NC_000004.11:g.24801871G= , CM000666.1:g.24801871G= | GRCh37 |
| NC_000004.10:g.24410969G= | NCBI36 |
| NG_012213.1:g.9787G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.*5G= MANE Select | ENSP00000371554.3:n.*5G= | |
| ENST00000382120.3:c.*5G= | ENSP00000371554.3:n.*5G= | |
| NM_003102.2:c.*5G= | NP_003093.2:n.*5G= | |
| XR_427488.1:n.918G= | ||
| NM_003102.3:c.*5G= | NP_003093.2:n.*5G= | |
| NM_003102.4:c.*5G= MANE Select | NP_003093.2:n.*5G= |