Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154837G= , CM000681.2:g.55154837G= | GRCh38 |
| NC_000019.9:g.55666205G= , CM000681.1:g.55666205G= | GRCh37 |
| NC_000019.8:g.60358017G= | NCBI36 |
| NG_007866.2:g.7896C= , LRG_432:g.7896C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.283-7C= MANE Select | ENSP00000341838.5:n.283-7C= | |
| ENST00000665070.1:c.283-7C= | ENSP00000499482.1:n.283-7C= | |
| ENST00000344887.9:c.283-7C= | ENSP00000341838.5:n.283-7C= | |
| ENST00000585806.5:n.282-7C= | ||
| ENST00000586669.5:n.291-7C= | ||
| ENST00000587176.5:n.467-7C= | ||
| ENST00000587871.1:c.902-7C= | ||
| ENST00000588882.1:c.208-7C= | ENSP00000466729.1:n.208-7C= | |
| ENST00000590463.1:n.455-7C= | ||
| NM_000363.4:c.283-7C= , LRG_432t1:c.283-7C= | NP_000354.4:n.283-7C= | |
| NM_000363.5:c.283-7C= MANE Select | NP_000354.4:n.283-7C= |