Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.173232402G= , CM000667.2:g.173232402G= | GRCh38 |
| NC_000005.9:g.172659405G= , CM000667.1:g.172659405G= | GRCh37 |
| NC_000005.8:g.172592011G= | NCBI36 |
| NG_013340.1:g.7911C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329198.5:c.*167C= MANE Select | ENSP00000327758.4:n.*167C= | |
| ENST00000329198.4:c.*167C= | ENSP00000327758.4:n.*167C= | |
| NM_001166175.1:c.*1095C= | NP_001159647.1:n.*1095C= | |
| NM_001166176.1:c.*941C= | NP_001159648.1:n.*941C= | |
| NM_004387.3:c.*167C= | NP_004378.1:n.*167C= | |
| NM_004387.4:c.*167C= MANE Select | NP_004378.1:n.*167C= | |
| NM_001166175.2:c.*1095C= | NP_001159647.1:n.*1095C= | |
| NM_001166176.2:c.*941C= | NP_001159648.1:n.*941C= |