Linked Data
ClinVar Variation Id:
386614
dbSNP Id:
rs753764564
ExAC:
11:68527684 C / T
gnomAD v2:
11-68527684-C-T
gnomAD v3:
11-68760216-C-T
gnomAD v4:
11-68760216-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68760216C>T , CM000673.2:g.68760216C>T | GRCh38 |
| NC_000011.9:g.68527684C>T , CM000673.1:g.68527684C>T | GRCh37 |
| NC_000011.8:g.68284260C>T | NCBI36 |
| NG_011801.1:g.86716G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265641.10:c.2142+9G>A MANE Select | ENSP00000265641.4:n.2142+9G>A | |
| ENST00000265641.9:c.2142+9G>A | ENSP00000265641.4:n.2142+9G>A | |
| ENST00000376618.6:c.2142+9G>A | ENSP00000365803.2:n.2142+9G>A | |
| ENST00000539743.5:c.2142+9G>A | ENSP00000446108.1:n.2142+9G>A | |
| ENST00000540367.5:c.2142+9G>A | ENSP00000439084.1:n.2142+9G>A | |
| NM_001031847.2:c.2142+9G>A | NP_001027017.1:n.2142+9G>A | |
| NM_001876.3:c.2142+9G>A | NP_001867.2:n.2142+9G>A | |
| XM_005273762.1:c.2238+9G>A | XP_005273819.1:n.2238+9G>A | |
| XM_005273763.1:c.2238+9G>A | XP_005273820.1:n.2238+9G>A | |
| XM_005273762.3:c.2238+9G>A | XP_005273819.1:n.2238+9G>A | |
| XM_017017220.1:c.2142+9G>A | XP_016872709.1:n.2142+9G>A | |
| NM_001876.4:c.2142+9G>A MANE Select | NP_001867.2:n.2142+9G>A | |
| NM_001031847.3:c.2142+9G>A | NP_001027017.1:n.2142+9G>A |