Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50924101C= , CM000676.2:g.50924101C= | GRCh38 |
| NC_000014.8:g.51390819C= , CM000676.1:g.51390819C= | GRCh37 |
| NC_000014.7:g.50460569C= | NCBI36 |
| NG_012796.1:g.25430G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216392.8:c.529-1G= MANE Select | ENSP00000216392.7:n.529-1G= | |
| ENST00000216392.7:c.529-1G= | ENSP00000216392.7:n.529-1G= | |
| ENST00000530336.2:n.596-1G= | ||
| ENST00000532462.5:c.529-1G= | ENSP00000431657.1:n.529-1G= | |
| ENST00000544180.6:c.427-1G= | ENSP00000443787.1:n.427-1G= | |
| NM_001163940.1:c.427-1G= | NP_001157412.1:n.427-1G= | |
| NM_002863.4:c.529-1G= | NP_002854.3:n.529-1G= | |
| NM_002863.5:c.529-1G= MANE Select | NP_002854.3:n.529-1G= | |
| NM_001163940.2:c.427-1G= | NP_001157412.1:n.427-1G= |