Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.173232542C= , CM000667.2:g.173232542C= | GRCh38 |
| NC_000005.9:g.172659545C= , CM000667.1:g.172659545C= | GRCh37 |
| NC_000005.8:g.172592151C= | NCBI36 |
| NG_013340.1:g.7771G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329198.5:c.*27G= MANE Select | ENSP00000327758.4:n.*27G= | |
| ENST00000329198.4:c.*27G= | ENSP00000327758.4:n.*27G= | |
| NM_001166175.1:c.*955G= | NP_001159647.1:n.*955G= | |
| NM_001166176.1:c.*801G= | NP_001159648.1:n.*801G= | |
| NM_004387.3:c.*27G= | NP_004378.1:n.*27G= | |
| NM_004387.4:c.*27G= MANE Select | NP_004378.1:n.*27G= | |
| NM_001166175.2:c.*955G= | NP_001159647.1:n.*955G= | |
| NM_001166176.2:c.*801G= | NP_001159648.1:n.*801G= |