Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67740517C= , CM000666.2:g.67740517C= | GRCh38 |
| NC_000004.11:g.68606235C= , CM000666.1:g.68606235C= | GRCh37 |
| NC_000004.10:g.68288830C= | NCBI36 |
| NG_009293.1:g.20570G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000226413.5:c.950G= MANE Select | ENSP00000226413.5:p.Cys317= | |
| ENST00000226413.4:c.950G= | ENSP00000226413.4:p.Cys317= | |
| ENST00000420975.2:c.822G= | ENSP00000397561.2:n.822G= | |
| NM_000406.2:c.950G= | NP_000397.1:p.Cys317= | |
| NM_001012763.1:c.*72G= | NP_001012781.1:n.*72G= | |
| NM_000406.3:c.950G= MANE Select | NP_000397.1:p.Cys317= | |
| NM_001012763.2:c.*72G= | NP_001012781.1:n.*72G= |