Linked Data
ClinVar Variation Id:
305854
dbSNP Id:
rs187924099
ExAC:
11:68704309 G / A
gnomAD v2:
11-68704309-G-A
gnomAD v3:
11-68936841-G-A
gnomAD v4:
11-68936841-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68936841G>A , CM000673.2:g.68936841G>A | GRCh38 |
| NC_000011.9:g.68704309G>A , CM000673.1:g.68704309G>A | GRCh37 |
| NC_000011.8:g.68460885G>A | NCBI36 |
| NG_007976.1:g.37991G>A , LRG_250:g.37991G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000255078.8:c.2361G>A MANE Select | ENSP00000255078.4:p.Pro787= | |
| ENST00000674675.1:c.587+18G>A | ||
| ENST00000674878.1:c.547+58G>A | ||
| ENST00000674955.1:c.*1078G>A | ENSP00000502463.1:n.*1078G>A | |
| ENST00000675118.1:c.1849G>A | ||
| ENST00000675389.1:n.636G>A | ||
| ENST00000675615.1:c.2361G>A | ENSP00000502413.1:p.Pro787= | |
| ENST00000675648.1:n.1736G>A | ||
| ENST00000675916.1:c.605G>A | ||
| ENST00000676173.1:n.3106G>A | ||
| ENST00000676182.1:c.792G>A | ||
| ENST00000676228.1:c.*1684G>A | ENSP00000502375.1:n.*1684G>A | |
| ENST00000255078.7:c.2361G>A | ENSP00000255078.3:p.Pro787= | |
| ENST00000539064.5:n.2120G>A | ||
| ENST00000543739.5:n.1354G>A | ||
| NM_002180.2:c.2361G>A , LRG_250t1:c.2361G>A | NP_002171.2:p.Pro787= | |
| XM_005273974.2:c.1350G>A | XP_005274031.1:p.Pro450= | |
| XM_005273975.2:c.1233G>A | XP_005274032.1:p.Pro411= | |
| XM_011544994.1:c.1128G>A | XP_011543296.1:p.Pro376= | |
| XR_949903.1:n.2463G>A | ||
| XM_005273975.3:c.1233G>A | XP_005274032.1:p.Pro411= | |
| XM_017017669.2:c.1350G>A | XP_016873158.1:p.Pro450= | |
| XM_017017670.2:c.1350G>A | XP_016873159.1:p.Pro450= | |
| XR_949903.3:n.2459G>A | ||
| NM_002180.3:c.2361G>A MANE Select | NP_002171.2:p.Pro787= |