Linked Data
ClinVar Variation Id:
2134614
ClinVar RCV Id:
RCV003058165
dbSNP Id:
rs1315751724
gnomAD v2:
4-17505983-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.17504360G>A , CM000666.2:g.17504360G>A | GRCh38 |
| NC_000004.11:g.17505983G>A , CM000666.1:g.17505983G>A | GRCh37 |
| NC_000004.10:g.17115081G>A | NCBI36 |
| NG_008763.1:g.12875C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706645.1:n.1342+19C>T | ||
| ENST00000281243.10:c.295+19C>T MANE Select | ENSP00000281243.5:n.295+19C>T | |
| ENST00000281243.9:c.295+19C>T | ENSP00000281243.5:n.295+19C>T | |
| ENST00000428702.6:c.202+19C>T | ENSP00000390944.2:n.202+19C>T | |
| ENST00000505710.1:c.222+19C>T | ||
| ENST00000507439.5:c.295+19C>T | ENSP00000423227.1:n.295+19C>T | |
| ENST00000508623.5:c.295+19C>T | ENSP00000426377.1:n.295+19C>T | |
| ENST00000513615.5:c.295+19C>T | ENSP00000422759.1:n.295+19C>T | |
| ENST00000514300.1:c.*226+19C>T | ENSP00000426039.1:n.*226+19C>T | |
| NM_000320.2:c.295+19C>T | NP_000311.2:n.295+19C>T | |
| NM_001306140.1:c.202+19C>T | NP_001293069.1:n.202+19C>T | |
| XR_241677.1:n.458+19C>T | ||
| NR_156494.1:n.475+19C>T | ||
| NM_000320.3:c.295+19C>T MANE Select | NP_000311.2:n.295+19C>T | |
| NM_001306140.2:c.202+19C>T | NP_001293069.1:n.202+19C>T | |
| NR_156494.2:n.331+19C>T |