Linked Data
ClinVar Variation Id:
9740
ClinVar RCV Id:
RCV000010393
dbSNP Id:
rs104894958
PubMed:
PMID:1639410
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.2787327G>A , CM000686.2:g.2787327G>A | GRCh38 |
| NC_000024.9:g.2655368G>A , CM000686.1:g.2655368G>A | GRCh37 |
| NC_000024.8:g.2715368G>A | NCBI36 |
| NG_011751.1:g.5425C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000679518.1:n.106+12588G>A | ||
| ENST00000679825.1:n.439G>A | ||
| ENST00000680285.1:n.320-2422G>A | ||
| ENST00000680845.1:n.166-153G>A | ||
| ENST00000681787.1:n.106+12588G>A | ||
| ENST00000681940.1:n.106+12588G>A | ||
| ENST00000383070.2:c.277C>T MANE Select | ENSP00000372547.1:p.Gln93Ter | |
| ENST00000383070.1:c.277C>T | ENSP00000372547.1:p.Gln93Ter | |
| NM_003140.2:c.277C>T | NP_003131.1:p.Gln93Ter | |
| NM_003140.3:c.277C>T MANE Select | NP_003131.1:p.Gln93Ter |