Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190408373A= , CM000665.2:g.190408373A= | GRCh38 |
| NC_000003.11:g.190126162A= , CM000665.1:g.190126162A= | GRCh37 |
| NC_000003.10:g.191608856A= | NCBI36 |
| NG_008149.1:g.25322A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.3:c.442A= MANE Select | ENSP00000264734.3:p.Thr148= | |
| ENST00000456423.2:c.115-1530A= | ENSP00000414136.2:n.115-1530A= | |
| ENST00000264734.2:c.652A= | ENSP00000264734.2:p.Thr218= | |
| ENST00000456423.1:c.325-1530A= | ENSP00000414136.1:n.325-1530A= | |
| NM_006580.3:c.652A= | NP_006571.1:p.Thr218= | |
| NM_001378492.1:c.442A= | NP_001365421.1:p.Thr148= | |
| NM_001378493.1:c.442A= | NP_001365422.1:p.Thr148= | |
| NM_006580.4:c.442A= MANE Select | NP_006571.2:p.Thr148= |