Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21174682C>A , CM000674.2:g.21174682C>A | GRCh38 |
| NC_000012.11:g.21327616C>A , CM000674.1:g.21327616C>A | GRCh37 |
| NC_000012.10:g.21218883C>A | NCBI36 |
| NG_011745.1:g.48489C>A , LRG_1022:g.48489C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.332C>A MANE Select | ENSP00000256958.2:p.Thr111Asn | |
| ENST00000256958.2:c.332C>A | ENSP00000256958.2:p.Thr111Asn | |
| ENST00000543498.5:c.426-2094C>A | ||
| NM_006446.4:c.332C>A , LRG_1022t1:c.332C>A | NP_006437.3:p.Thr111Asn | |
| NM_006446.5:c.332C>A MANE Select | NP_006437.3:p.Thr111Asn |