Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.139373033A= , CM000668.2:g.139373033A= | GRCh38 |
| NC_000006.11:g.139694170A= , CM000668.1:g.139694170A= | GRCh37 |
| NC_000006.10:g.139735863A= | NCBI36 |
| NG_016169.1:g.6616T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367651.4:c.*99T= MANE Select | ENSP00000356623.2:n.*99T= | |
| ENST00000367651.3:c.*99T= | ENSP00000356623.2:n.*99T= | |
| ENST00000536159.2:c.*99T= | ENSP00000442831.1:n.*99T= | |
| ENST00000537332.2:c.*99T= | ENSP00000444198.2:n.*99T= | |
| NM_001168388.2:c.*99T= | NP_001161860.1:n.*99T= | |
| NM_001168389.2:c.*99T= | NP_001161861.2:n.*99T= | |
| NM_006079.4:c.*99T= | NP_006070.2:n.*99T= | |
| NM_006079.5:c.*99T= MANE Select | NP_006070.2:n.*99T= | |
| NM_001168388.3:c.*99T= | NP_001161860.1:n.*99T= | |
| NM_001168389.3:c.*99T= | NP_001161861.2:n.*99T= |