Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21174488T= , CM000674.2:g.21174488T= | GRCh38 |
| NC_000012.11:g.21327422T= , CM000674.1:g.21327422T= | GRCh37 |
| NC_000012.10:g.21218689T= | NCBI36 |
| NG_011745.1:g.48295T= , LRG_1022:g.48295T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.227-89T= MANE Select | ENSP00000256958.2:n.227-89T= | |
| ENST00000256958.2:c.227-89T= | ENSP00000256958.2:n.227-89T= | |
| ENST00000543498.5:c.426-2288T= | ||
| NM_006446.4:c.227-89T= , LRG_1022t1:c.227-89T= | NP_006437.3:n.227-89T= | |
| NM_006446.5:c.227-89T= MANE Select | NP_006437.3:n.227-89T= |