Linked Data
ClinVar Variation Id:
536719
dbSNP Id:
rs762594014
ExAC:
10:75860765 C / T
gnomAD v2:
10-75860765-C-T
gnomAD v3:
10-74101007-C-T
gnomAD v4:
10-74101007-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.74101007C>T , CM000672.2:g.74101007C>T | GRCh38 |
| NC_000010.10:g.75860765C>T , CM000672.1:g.75860765C>T | GRCh37 |
| NC_000010.9:g.75530771C>T | NCBI36 |
| NG_008868.1:g.107894C>T , LRG_383:g.107894C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000211998.10:c.1932C>T MANE Select | ENSP00000211998.5:p.Ala644= | |
| ENST00000211998.8:c.1932C>T | ENSP00000211998.4:p.Ala644= | |
| ENST00000372755.7:c.1932C>T | ENSP00000361841.3:p.Ala644= | |
| ENST00000436396.1:c.948C>T | ENSP00000415489.1:p.Ala316= | |
| ENST00000478896.2:n.332-47C>T | ||
| ENST00000623461.3:n.4735C>T | ||
| ENST00000624354.3:c.*1687C>T | ENSP00000485551.1:n.*1687C>T | |
| NM_003373.3:c.1932C>T | NP_003364.1:p.Ala644= | |
| NM_014000.2:c.1932C>T , LRG_383t1:c.1932C>T | NP_054706.1:p.Ala644= | |
| XM_005270142.1:c.1935C>T | XP_005270199.1:p.Ala645= | |
| XM_005270143.1:c.1935C>T | XP_005270200.1:p.Ala645= | |
| NM_003373.4:c.1932C>T | NP_003364.1:p.Ala644= | |
| NM_014000.3:c.1932C>T MANE Select | NP_054706.1:p.Ala644= |