Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.67259132T= , CM000663.2:g.67259132T= | GRCh38 |
| NC_000001.10:g.67724815T= , CM000663.1:g.67724815T= | GRCh37 |
| NC_000001.9:g.67497403T= | NCBI36 |
| NG_011498.1:g.97647T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000347310.10:c.*4T= MANE Select | ENSP00000321345.5:n.*4T= | |
| ENST00000637002.1:c.*4T= | ENSP00000490340.1:n.*4T= | |
| ENST00000347310.9:c.*4T= | ENSP00000321345.5:n.*4T= | |
| ENST00000395227.2:c.*4T= | ENSP00000378652.2:n.*4T= | |
| ENST00000425614.3:c.*4T= | ENSP00000387640.2:n.*4T= | |
| ENST00000473881.2:c.*720T= | ENSP00000486667.1:n.*720T= | |
| NM_144701.2:c.*4T= | NP_653302.2:n.*4T= | |
| XM_005270516.2:c.*4T= | XP_005270573.1:n.*4T= | |
| XM_011540789.1:c.*4T= | XP_011539091.1:n.*4T= | |
| XM_011540790.1:c.*4T= | XP_011539092.1:n.*4T= | |
| XM_011540791.1:c.*4T= | XP_011539093.1:n.*4T= | |
| XM_011540790.3:c.*4T= | XP_011539092.1:n.*4T= | |
| XM_011540791.3:c.*4T= | XP_011539093.1:n.*4T= | |
| NM_144701.3:c.*4T= MANE Select | NP_653302.2:n.*4T= |