Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.104956438T= , CM000668.2:g.104956438T= | GRCh38 |
| NC_000006.11:g.105404313T= , CM000668.1:g.105404313T= | GRCh37 |
| NC_000006.10:g.105511006T= | NCBI36 |
| NG_032815.1:g.4391T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000635857.1:c.68-1661T= | ENSP00000489735.1:n.68-1661T= | |
| ENST00000637759.1:c.35-1661T= | ENSP00000490468.1:n.35-1661T= | |
| XM_006715477.2:c.68-1661T= | XP_006715540.2:n.68-1661T= | |
| XM_011535818.1:c.35-1661T= | XP_011534120.1:n.35-1661T= | |
| XM_011535818.3:c.35-1661T= | XP_011534120.1:n.35-1661T= |