Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.25869178C= , CM000668.2:g.25869178C= | GRCh38 |
| NC_000006.11:g.25869406C= , CM000668.1:g.25869406C= | GRCh37 |
| NC_000006.10:g.25977385C= | NCBI36 |
| NG_032922.1:g.10066G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360657.7:c.-33-758G= | ENSP00000353873.3:n.-33-758G= | |
| ENST00000361703.10:c.-33-758G= | ENSP00000355307.6:n.-33-758G= | |
| ENST00000397060.8:c.-33-758G= MANE Select | ENSP00000380250.4:n.-33-758G= | |
| ENST00000503922.5:n.73-758G= | ||
| ENST00000506105.5:c.-33-758G= | ENSP00000424729.1:n.-33-758G= | |
| NM_001098486.1:c.-33-758G= | NP_001091956.1:n.-33-758G= | |
| NM_006632.3:c.-33-758G= | NP_006623.2:n.-33-758G= | |
| NM_001098486.2:c.-33-758G= MANE Select | NP_001091956.1:n.-33-758G= | |
| NM_006632.4:c.-33-758G= | NP_006623.2:n.-33-758G= |