Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21174648G>T , CM000674.2:g.21174648G>T | GRCh38 |
| NC_000012.11:g.21327582G>T , CM000674.1:g.21327582G>T | GRCh37 |
| NC_000012.10:g.21218849G>T | NCBI36 |
| NG_011745.1:g.48455G>T , LRG_1022:g.48455G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.298G>T MANE Select | ENSP00000256958.2:p.Gly100Cys | |
| ENST00000256958.2:c.298G>T | ENSP00000256958.2:p.Gly100Cys | |
| ENST00000543498.5:c.426-2128G>T | ||
| NM_006446.4:c.298G>T , LRG_1022t1:c.298G>T | NP_006437.3:p.Gly100Cys | |
| NM_006446.5:c.298G>T MANE Select | NP_006437.3:p.Gly100Cys |