Linked Data
ClinVar Variation Id:
2934680
ClinVar RCV Id:
RCV003798382
dbSNP Id:
rs1289494832
gnomAD v2:
11-68704120-T-C
gnomAD v4:
11-68936652-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68936652T>C , CM000673.2:g.68936652T>C | GRCh38 |
| NC_000011.9:g.68704120T>C , CM000673.1:g.68704120T>C | GRCh37 |
| NC_000011.8:g.68460696T>C | NCBI36 |
| NG_007976.1:g.37802T>C , LRG_250:g.37802T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000255078.8:c.2172T>C MANE Select | ENSP00000255078.4:p.Asp724= | |
| ENST00000674675.1:c.416T>C | ||
| ENST00000674878.1:c.416T>C | ||
| ENST00000674955.1:c.*889T>C | ENSP00000502463.1:n.*889T>C | |
| ENST00000675118.1:c.1660T>C | ||
| ENST00000675389.1:n.447T>C | ||
| ENST00000675615.1:c.2172T>C | ENSP00000502413.1:p.Asp724= | |
| ENST00000675648.1:n.1547T>C | ||
| ENST00000675916.1:c.416T>C | ||
| ENST00000676173.1:n.2917T>C | ||
| ENST00000676182.1:c.603T>C | ||
| ENST00000676228.1:c.*1495T>C | ENSP00000502375.1:n.*1495T>C | |
| ENST00000255078.7:c.2172T>C | ENSP00000255078.3:p.Asp724= | |
| ENST00000539064.5:n.1931T>C | ||
| ENST00000543739.5:n.1165T>C | ||
| NM_002180.2:c.2172T>C , LRG_250t1:c.2172T>C | NP_002171.2:p.Asp724= | |
| XM_005273974.2:c.1161T>C | XP_005274031.1:p.Asp387= | |
| XM_005273975.2:c.1044T>C | XP_005274032.1:p.Asp348= | |
| XM_011544994.1:c.939T>C | XP_011543296.1:p.Asp313= | |
| XR_949903.1:n.2274T>C | ||
| XM_005273975.3:c.1044T>C | XP_005274032.1:p.Asp348= | |
| XM_017017669.2:c.1161T>C | XP_016873158.1:p.Asp387= | |
| XM_017017670.2:c.1161T>C | XP_016873159.1:p.Asp387= | |
| XR_949903.3:n.2270T>C | ||
| NM_002180.3:c.2172T>C MANE Select | NP_002171.2:p.Asp724= |