Linked Data
ClinVar Variation Id:
9738
ClinVar RCV Id:
RCV000010391
dbSNP Id:
rs104894956
PubMed:
PMID:1483689
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.2787278A>G , CM000686.2:g.2787278A>G | GRCh38 |
| NC_000024.9:g.2655319A>G , CM000686.1:g.2655319A>G | GRCh37 |
| NC_000024.8:g.2715319A>G | NCBI36 |
| NG_011751.1:g.5474T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000679518.1:n.106+12539A>G | ||
| ENST00000679825.1:n.390A>G | ||
| ENST00000680285.1:n.320-2471A>G | ||
| ENST00000680845.1:n.166-202A>G | ||
| ENST00000681787.1:n.106+12539A>G | ||
| ENST00000681940.1:n.106+12539A>G | ||
| ENST00000383070.2:c.326T>C MANE Select | ENSP00000372547.1:p.Phe109Ser | |
| ENST00000383070.1:c.326T>C | ENSP00000372547.1:p.Phe109Ser | |
| NM_003140.2:c.326T>C | NP_003131.1:p.Phe109Ser | |
| NM_003140.3:c.326T>C MANE Select | NP_003131.1:p.Phe109Ser |