Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.109766952T= , CM000675.2:g.109766952T= | GRCh38 |
| NC_000013.10:g.110419299T= , CM000675.1:g.110419299T= | GRCh37 |
| NC_000013.9:g.109217300T= | NCBI36 |
| NG_008154.1:g.24616A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375856.5:c.4013-10644A= MANE Select | ENSP00000365016.3:n.4013-10644A= | |
| ENST00000375856.4:c.4013-10644A= | ENSP00000365016.3:n.4013-10644A= | |
| NM_003749.2:c.4013-10644A= | NP_003740.2:n.4013-10644A= | |
| NM_003749.3:c.4013-10644A= MANE Select | NP_003740.2:n.4013-10644A= |