Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.104954208C= , CM000668.2:g.104954208C= | GRCh38 |
| NC_000006.11:g.105402083C= , CM000668.1:g.105402083C= | GRCh37 |
| NC_000006.10:g.105508776C= | NCBI36 |
| NG_032815.1:g.2161C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000635857.1:c.67+3699C= | ENSP00000489735.1:n.67+3699C= | |
| ENST00000637759.1:c.34+3699C= | ENSP00000490468.1:n.34+3699C= | |
| XM_006715477.2:c.67+3699C= | XP_006715540.2:n.67+3699C= | |
| XM_011535818.1:c.34+3699C= | XP_011534120.1:n.34+3699C= | |
| XM_011535818.3:c.34+3699C= | XP_011534120.1:n.34+3699C= |