Linked Data
ClinVar Variation Id:
370865
dbSNP Id:
rs1057516825
gnomAD v4:
8-86628918-C-T
PubMed:
PMID:28795510
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86628918C>T , CM000670.2:g.86628918C>T | GRCh38 |
| NC_000008.10:g.87641146C>T , CM000670.1:g.87641146C>T | GRCh37 |
| NC_000008.9:g.87710262C>T | NCBI36 |
| NG_016980.1:g.119758G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320005.6:c.1480+1G>A MANE Select | ENSP00000316605.5:n.1480+1G>A | |
| ENST00000681546.1:n.1300+1G>A | ||
| ENST00000681746.1:c.1480+1G>A | ENSP00000505959.1:n.1480+1G>A | |
| ENST00000320005.5:c.1480+1G>A | ENSP00000316605.5:n.1480+1G>A | |
| NM_019098.4:c.1480+1G>A | NP_061971.3:n.1480+1G>A | |
| XM_011517138.1:c.1066+1G>A | XP_011515440.1:n.1066+1G>A | |
| XM_011517138.2:c.1066+1G>A | XP_011515440.1:n.1066+1G>A | |
| NM_019098.5:c.1480+1G>A MANE Select | NP_061971.3:n.1480+1G>A |