Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229431713C= , CM000663.2:g.229431713C= | GRCh38 |
| NC_000001.10:g.229567460C= , CM000663.1:g.229567460C= | GRCh37 |
| NC_000001.9:g.227634083C= | NCBI36 |
| NG_006672.1:g.7384G= , LRG_429:g.7384G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366683.4:c.990+8G= | ENSP00000355644.4:n.990+8G= | |
| ENST00000684723.1:c.855+8G= | ENSP00000508084.1:n.855+8G= | |
| ENST00000366683.3:c.621+8G= | ENSP00000355644.3:n.621+8G= | |
| ENST00000366684.7:c.990+8G= MANE Select | ENSP00000355645.3:n.990+8G= | |
| NM_001100.3:c.990+8G= , LRG_429t1:c.990+8G= | NP_001091.1:n.990+8G= | |
| NM_001100.4:c.990+8G= MANE Select | NP_001091.1:n.990+8G= |