Linked Data
ClinVar Variation Id:
2862048
ClinVar RCV Id:
RCV003704615
MyVariant Identifiers:
chr17:g.74536238T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.76540156T>G , CM000679.2:g.76540156T>G | GRCh38 |
| NC_000017.10:g.74536238T>G , CM000679.1:g.74536238T>G | GRCh37 |
| NC_000017.9:g.72047833T>G | NCBI36 |
| NG_016702.1:g.17571T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000592014.6:c.15T>G (PRCD) MANE Select | ENSP00000467661.1:p.Leu5= | |
| ENST00000397633.7:n.46-349T>G (PRCD) | ||
| ENST00000465808.7:n.93-349T>G (PRCD) | ||
| ENST00000586148.1:c.15T>G (PRCD) | ENSP00000465932.1:p.Leu5= | |
| ENST00000589145.1:c.-52-8465A>C (CYGB) | ENSP00000468559.1:n.-52-8465A>C | |
| ENST00000590555.5:n.445-349T>G (PRCD) | ||
| ENST00000592014.5:c.15T>G (PRCD) | ENSP00000467661.1:p.Leu5= | |
| ENST00000592432.5:n.249-349T>G (PRCD) | ||
| NM_001077620.2:c.15T>G (PRCD) | NP_001071088.1:p.Leu5= | |
| NR_033357.1:n.249-349T>G (PRCD) | ||
| XM_011524272.1:c.-52-8465A>C (CYGB) | XP_011522574.1:n.-52-8465A>C | |
| XM_011525184.1:c.138T>G (PRCD) | XP_011523486.1:p.Leu46= | |
| XM_017024116.1:c.-52-8465A>C (CYGB) | XP_016879605.1:n.-52-8465A>C | |
| XM_017025013.1:c.15T>G (PRCD) | XP_016880502.1:p.Leu5= | |
| XM_017025014.1:c.15T>G (PRCD) | XP_016880503.1:p.Leu5= | |
| XM_017025015.1:c.15T>G (PRCD) | XP_016880504.1:p.Leu5= | |
| NM_001077620.3:c.15T>G (PRCD) MANE Select | NP_001071088.1:p.Leu5= | |
| NR_033357.2:n.249-349T>G (PRCD) |