Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.30606952G>T , CM000665.2:g.30606952G>T | GRCh38 |
| NC_000003.11:g.30648444G>T , CM000665.1:g.30648444G>T | GRCh37 |
| NC_000003.10:g.30623448G>T | NCBI36 |
| NG_007490.1:g.5451G>T , LRG_779:g.5451G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003242.6:c.69G>T MANE Select | NP_003233.4:p.Thr23= |
| ENST00000295754.10:c.69G>T MANE Select | ENSP00000295754.5:p.Thr23= |
| NM_001024847.2:c.69G>T , LRG_779t1:c.69G>T | NP_001020018.1:p.Thr23= |
| NM_003242.5:c.69G>T | NP_003233.4:p.Thr23= |
| ENST00000295754.9:c.69G>T | ENSP00000295754.5:p.Thr23= |
| ENST00000359013.4:c.69G>T | ENSP00000351905.4:p.Thr23= |
| XM_011534045.1:c.-12+359G>T | XP_011532347.1:n.-12+359G>T |
| XM_011534045.3:c.-12+359G>T | XP_011532347.1:n.-12+359G>T |