Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.2787566T>G , CM000686.2:g.2787566T>G | GRCh38 |
| NC_000024.9:g.2655607T>G , CM000686.1:g.2655607T>G | GRCh37 |
| NC_000024.8:g.2715607T>G | NCBI36 |
| NG_011751.1:g.5186A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000679518.1:n.106+12827T>G | ||
| ENST00000679825.1:n.678T>G | ||
| ENST00000680285.1:n.320-2183T>G | ||
| ENST00000680845.1:n.252T>G | ||
| ENST00000681787.1:n.106+12827T>G | ||
| ENST00000681940.1:n.106+12827T>G | ||
| ENST00000383070.2:c.38A>C MANE Select | ENSP00000372547.1:p.Asn13Thr | |
| ENST00000383070.1:c.38A>C | ENSP00000372547.1:p.Asn13Thr | |
| NM_003140.2:c.38A>C | NP_003131.1:p.Asn13Thr | |
| NM_003140.3:c.38A>C MANE Select | NP_003131.1:p.Asn13Thr |