Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.2787136T>G , CM000686.2:g.2787136T>G | GRCh38 |
| NC_000024.9:g.2655177T>G , CM000686.1:g.2655177T>G | GRCh37 |
| NC_000024.8:g.2715177T>G | NCBI36 |
| NG_011751.1:g.5616A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000679518.1:n.106+12397T>G | ||
| ENST00000679825.1:n.248T>G | ||
| ENST00000680285.1:n.320-2613T>G | ||
| ENST00000680845.1:n.165+83T>G | ||
| ENST00000681787.1:n.106+12397T>G | ||
| ENST00000681940.1:n.106+12397T>G | ||
| ENST00000383070.2:c.468A>C MANE Select | ENSP00000372547.1:p.Glu156Asp | |
| ENST00000383070.1:c.468A>C | ENSP00000372547.1:p.Glu156Asp | |
| NM_003140.2:c.468A>C | NP_003131.1:p.Glu156Asp | |
| NM_003140.3:c.468A>C MANE Select | NP_003131.1:p.Glu156Asp |