Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.30606666G= , CM000665.2:g.30606666G= | GRCh38 |
| NC_000003.11:g.30648158G= , CM000665.1:g.30648158G= | GRCh37 |
| NC_000003.10:g.30623162G= | NCBI36 |
| NG_007490.1:g.5165G= , LRG_779:g.5165G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295754.10:c.-218G= MANE Select | ENSP00000295754.5:n.-218G= | |
| ENST00000295754.9:c.-218G= | ENSP00000295754.5:n.-218G= | |
| ENST00000359013.4:c.-218G= | ENSP00000351905.4:n.-218G= | |
| NM_001024847.2:c.-218G= , LRG_779t1:c.-218G= | NP_001020018.1:n.-218G= | |
| NM_003242.5:c.-218G= | NP_003233.4:n.-218G= | |
| XM_011534045.1:c.-12+73G= | XP_011532347.1:n.-12+73G= | |
| XM_011534045.3:c.-12+73G= | XP_011532347.1:n.-12+73G= | |
| NM_003242.6:c.-218G= MANE Select | NP_003233.4:n.-218G= |