Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21178396T= , CM000674.2:g.21178396T= | GRCh38 |
| NC_000012.11:g.21331330T= , CM000674.1:g.21331330T= | GRCh37 |
| NC_000012.10:g.21222597T= | NCBI36 |
| NG_011745.1:g.52203T= , LRG_1022:g.52203T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.482-180T= MANE Select | ENSP00000256958.2:n.482-180T= | |
| ENST00000256958.2:c.482-180T= | ENSP00000256958.2:n.482-180T= | |
| NM_006446.4:c.482-180T= , LRG_1022t1:c.482-180T= | NP_006437.3:n.482-180T= | |
| NM_006446.5:c.482-180T= MANE Select | NP_006437.3:n.482-180T= |