Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.173232541T>G , CM000667.2:g.173232541T>G | GRCh38 |
| NC_000005.9:g.172659544T>G , CM000667.1:g.172659544T>G | GRCh37 |
| NC_000005.8:g.172592150T>G | NCBI36 |
| NG_013340.1:g.7772A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329198.5:c.*28A>C MANE Select | ENSP00000327758.4:n.*28A>C | |
| ENST00000329198.4:c.*28A>C | ENSP00000327758.4:n.*28A>C | |
| NM_001166175.1:c.*956A>C | NP_001159647.1:n.*956A>C | |
| NM_001166176.1:c.*802A>C | NP_001159648.1:n.*802A>C | |
| NM_004387.3:c.*28A>C | NP_004378.1:n.*28A>C | |
| NM_004387.4:c.*28A>C MANE Select | NP_004378.1:n.*28A>C | |
| NM_001166175.2:c.*956A>C | NP_001159647.1:n.*956A>C | |
| NM_001166176.2:c.*802A>C | NP_001159648.1:n.*802A>C |