Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102852954G= , CM000674.2:g.102852954G= | GRCh38 |
| NC_000012.11:g.103246732G= , CM000674.1:g.103246732G= | GRCh37 |
| NC_000012.10:g.101770862G= | NCBI36 |
| NG_008690.1:g.69649C= | |
| NG_008690.2:g.110457C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553106.6:c.707-4C= MANE Select | ENSP00000448059.1:n.707-4C= | |
| ENST00000307000.7:c.692-4C= | ENSP00000303500.2:n.692-4C= | |
| ENST00000549247.6:n.462C= | ||
| ENST00000553106.5:c.707-4C= | ENSP00000448059.1:n.707-4C= | |
| NM_000277.1:c.707-4C= | NP_000268.1:n.707-4C= | |
| XM_011538422.1:c.707-4C= | XP_011536724.1:n.707-4C= | |
| NM_000277.2:c.707-4C= | NP_000268.1:n.707-4C= | |
| NM_001354304.1:c.707-4C= | NP_001341233.1:n.707-4C= | |
| NM_000277.3:c.707-4C= MANE Select | NP_000268.1:n.707-4C= | |
| NM_001354304.2:c.707-4C= | NP_001341233.1:n.707-4C= |