Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.101452774G= , CM000673.2:g.101452774G= | GRCh38 |
| NC_000011.9:g.101323505G= , CM000673.1:g.101323505G= | GRCh37 |
| NC_000011.8:g.100828715G= | NCBI36 |
| NG_011476.1:g.136155C= | |
| NG_011476.2:g.136155C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344327.8:c.*181C= MANE Select | ENSP00000340913.3:n.*181C= | |
| ENST00000344327.7:c.*181C= | ENSP00000340913.3:n.*181C= | |
| NM_004621.5:c.*181C= | NP_004612.2:n.*181C= | |
| XM_006718898.2:c.*181C= | XP_006718961.1:n.*181C= | |
| XM_011542968.1:c.*181C= | XP_011541270.1:n.*181C= | |
| XM_011542968.3:c.*181C= | XP_011541270.1:n.*181C= | |
| XM_017018221.2:c.*181C= | XP_016873710.1:n.*181C= | |
| XR_001747948.2:n.3334C= | ||
| NM_004621.6:c.*181C= MANE Select | NP_004612.2:n.*181C= |