Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.203960563T= , CM000664.2:g.203960563T= | GRCh38 |
| NC_000002.11:g.204825286T= , CM000664.1:g.204825286T= | GRCh37 |
| NC_000002.10:g.204533531T= | NCBI36 |
| NG_011586.1:g.28784T= , LRG_65:g.28784T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316386.11:c.*964T= MANE Select | ENSP00000319476.6:n.*964T= | |
| ENST00000316386.10:c.*964T= | ENSP00000319476.6:n.*964T= | |
| ENST00000435193.1:c.*972T= | ENSP00000415951.1:n.*972T= | |
| NM_012092.3:c.*964T= , LRG_65t1:c.*964T= | NP_036224.1:n.*964T= | |
| XM_011511028.1:c.*1065T= | XP_011509330.1:n.*1065T= | |
| XM_011511029.1:c.*964T= | XP_011509331.1:n.*964T= | |
| XM_011511030.1:c.*1065T= | XP_011509332.1:n.*1065T= | |
| XM_011511031.1:c.*1065T= | XP_011509333.1:n.*1065T= | |
| NM_012092.4:c.*964T= MANE Select | NP_036224.1:n.*964T= |