Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190388333A= , CM000665.2:g.190388333A= | GRCh38 |
| NC_000003.11:g.190106122A= , CM000665.1:g.190106122A= | GRCh37 |
| NC_000003.10:g.191588816A= | NCBI36 |
| NG_008149.1:g.5282A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264734.3:c.4A= MANE Select | ENSP00000264734.3:p.Arg2= | |
| ENST00000456423.2:c.4A= | ENSP00000414136.2:p.Arg2= | |
| ENST00000264734.2:c.214A= | ENSP00000264734.2:p.Arg72= | |
| ENST00000456423.1:c.214A= | ENSP00000414136.1:p.Arg72= | |
| ENST00000468220.1:n.306+13730A= | ||
| NM_006580.3:c.214A= | NP_006571.1:p.Arg72= | |
| NM_001378492.1:c.4A= | NP_001365421.1:p.Arg2= | |
| NM_001378493.1:c.4A= | NP_001365422.1:p.Arg2= | |
| NM_006580.4:c.4A= MANE Select | NP_006571.2:p.Arg2= |