Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23573158T= , CM000684.2:g.23573158T= | GRCh38 |
| NC_000022.10:g.23915345T= , CM000684.1:g.23915345T= | GRCh37 |
| NC_000022.9:g.22245345T= | NCBI36 |
| NG_009791.1:g.12151A= , LRG_69:g.12151A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330377.3:c.*108A= MANE Select | ENSP00000329312.2:n.*108A= | |
| ENST00000249053.3:c.*379A= | ENSP00000249053.3:n.*379A= | |
| ENST00000330377.2:c.*108A= | ENSP00000329312.2:n.*108A= | |
| NM_020070.3:c.*108A= | NP_064455.1:n.*108A= | |
| NM_152855.2:c.*379A= | NP_690594.1:n.*379A= | |
| XM_011530169.1:c.*108A= | XP_011528471.1:n.*108A= | |
| XM_011530169.2:c.*108A= | XP_011528471.1:n.*108A= | |
| NM_020070.4:c.*108A= MANE Select | NP_064455.1:n.*108A= | |
| NM_001369906.1:c.*108A= | NP_001356835.1:n.*108A= | |
| NM_152855.3:c.*379A= | NP_690594.1:n.*379A= |