Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28845287T= , CM000678.2:g.28845287T= | GRCh38 |
| NC_000016.9:g.28856608T= , CM000678.1:g.28856608T= | GRCh37 |
| NC_000016.8:g.28764109T= | NCBI36 |
| NG_008964.1:g.6122A= | |
| NG_029706.2:g.3688T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313511.8:c.414+27A= MANE Select | ENSP00000322439.3:n.414+27A= | |
| ENST00000313511.7:c.414+27A= | ENSP00000322439.3:n.414+27A= | |
| ENST00000565012.1:c.248-232A= | ENSP00000455007.1:n.248-232A= | |
| NM_003321.4:c.414+27A= | NP_003312.3:n.414+27A= | |
| XM_011545928.1:c.414+27A= | XP_011544230.1:n.414+27A= | |
| NM_001365360.1:c.414+27A= | NP_001352289.1:n.414+27A= | |
| NM_003321.5:c.414+27A= MANE Select | NP_003312.3:n.414+27A= | |
| NM_001365360.2:c.414+27A= | NP_001352289.1:n.414+27A= |