Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41623921A= , CM000679.2:g.41623921A= | GRCh38 |
| NC_000017.10:g.39780173A= , CM000679.1:g.39780173A= | GRCh37 |
| NC_000017.9:g.37033699A= | NCBI36 |
| NG_008625.1:g.5710T= | |
| NG_009090.2:g.167792T= , LRG_401:g.167792T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.432+157T= MANE Select | ENSP00000308452.8:n.432+157T= | |
| ENST00000311208.12:c.432+157T= | ENSP00000308452.8:n.432+157T= | |
| ENST00000463128.5:c.-184+157T= | ENSP00000468672.1:n.-184+157T= | |
| ENST00000491673.1:n.498+157T= | ||
| ENST00000493253.5:n.219+157T= | ||
| ENST00000540235.5:c.183+157T= | ENSP00000441751.2:n.183+157T= | |
| ENST00000577817.3:c.387+157T= | ENSP00000467418.1:n.387+157T= | |
| NM_000422.2:c.432+157T= | NP_000413.1:n.432+157T= | |
| NM_000422.3:c.432+157T= MANE Select | NP_000413.1:n.432+157T= |