Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.30606735G= , CM000665.2:g.30606735G= | GRCh38 |
| NC_000003.11:g.30648227G= , CM000665.1:g.30648227G= | GRCh37 |
| NC_000003.10:g.30623231G= | NCBI36 |
| NG_007490.1:g.5234G= , LRG_779:g.5234G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295754.10:c.-149G= MANE Select | ENSP00000295754.5:n.-149G= | |
| ENST00000295754.9:c.-149G= | ENSP00000295754.5:n.-149G= | |
| ENST00000359013.4:c.-149G= | ENSP00000351905.4:n.-149G= | |
| NM_001024847.2:c.-149G= , LRG_779t1:c.-149G= | NP_001020018.1:n.-149G= | |
| NM_003242.5:c.-149G= | NP_003233.4:n.-149G= | |
| XM_011534045.1:c.-12+142G= | XP_011532347.1:n.-12+142G= | |
| XM_011534045.3:c.-12+142G= | XP_011532347.1:n.-12+142G= | |
| NM_003242.6:c.-149G= MANE Select | NP_003233.4:n.-149G= |