Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190388262C>T , CM000665.2:g.190388262C>T | GRCh38 |
| NC_000003.11:g.190106051C>T , CM000665.1:g.190106051C>T | GRCh37 |
| NC_000003.10:g.191588745C>T | NCBI36 |
| NG_008149.1:g.5211C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.3:c.-68C>T MANE Select | ENSP00000264734.3:n.-68C>T | |
| ENST00000456423.2:c.-68C>T | ENSP00000414136.2:n.-68C>T | |
| ENST00000264734.2:c.143C>T | ENSP00000264734.2:p.Thr48Ile | |
| ENST00000456423.1:c.143C>T | ENSP00000414136.1:p.Thr48Ile | |
| ENST00000468220.1:n.306+13659C>T | ||
| NM_006580.3:c.143C>T | NP_006571.1:p.Thr48Ile | |
| NM_001378492.1:c.-68C>T | NP_001365421.1:n.-68C>T | |
| NM_001378493.1:c.-68C>T | NP_001365422.1:n.-68C>T | |
| NM_006580.4:c.-68C>T MANE Select | NP_006571.2:n.-68C>T |