Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154838A= , CM000681.2:g.55154838A= | GRCh38 |
| NC_000019.9:g.55666206A= , CM000681.1:g.55666206A= | GRCh37 |
| NC_000019.8:g.60358018A= | NCBI36 |
| NG_007866.2:g.7895T= , LRG_432:g.7895T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.283-8T= MANE Select | ENSP00000341838.5:n.283-8T= | |
| ENST00000665070.1:c.283-8T= | ENSP00000499482.1:n.283-8T= | |
| ENST00000344887.9:c.283-8T= | ENSP00000341838.5:n.283-8T= | |
| ENST00000585806.5:n.282-8T= | ||
| ENST00000586669.5:n.291-8T= | ||
| ENST00000587176.5:n.467-8T= | ||
| ENST00000587871.1:c.902-8T= | ||
| ENST00000588882.1:c.208-8T= | ENSP00000466729.1:n.208-8T= | |
| ENST00000590463.1:n.455-8T= | ||
| NM_000363.4:c.283-8T= , LRG_432t1:c.283-8T= | NP_000354.4:n.283-8T= | |
| NM_000363.5:c.283-8T= MANE Select | NP_000354.4:n.283-8T= |