Linked Data
ClinVar Variation Id:
1569409
ClinVar RCV Id:
RCV002220653
dbSNP Id:
rs2149841585
gnomAD v4:
5-132589819-C-T
MyVariant Identifiers:
chr5:g.131925511C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132589819C>T , CM000667.2:g.132589819C>T | GRCh38 |
| NC_000005.9:g.131925511C>T , CM000667.1:g.131925511C>T | GRCh37 |
| NC_000005.8:g.131953410C>T | NCBI36 |
| NG_021151.1:g.37896C>T | |
| NG_021151.2:g.37843C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378823.8:c.1434C>T MANE Select | ENSP00000368100.4:p.Asp478= | |
| ENST00000638452.2:c.1137C>T | ENSP00000492349.2:p.Asp379= | |
| ENST00000638504.1:n.1120C>T | ||
| ENST00000638568.2:c.1137C>T | ENSP00000491158.2:p.Asp379= | |
| ENST00000639899.1:n.1953C>T | ||
| ENST00000640655.2:c.1137C>T | ENSP00000491596.2:p.Asp379= | |
| ENST00000651160.1:c.1434C>T | ENSP00000498829.1:p.Asp478= | |
| ENST00000651541.1:c.1137C>T | ENSP00000498795.1:p.Asp379= | |
| ENST00000651658.1:n.1861C>T | ||
| ENST00000651723.1:c.*1517C>T | ENSP00000498237.1:n.*1517C>T | |
| ENST00000652016.1:c.1434C>T | ENSP00000498267.1:p.Asp478= | |
| ENST00000652485.1:c.1434C>T | ENSP00000498973.1:p.Asp478= | |
| ENST00000378823.7:c.1434C>T | ENSP00000368100.4:p.Asp478= | |
| ENST00000423956.5:c.1434C>T | ENSP00000390971.1:p.Asp478= | |
| ENST00000453394.5:c.1434C>T | ENSP00000400049.1:p.Asp478= | |
| ENST00000533482.5:c.*1060C>T | ENSP00000431225.1:n.*1060C>T | |
| NM_005732.3:c.1434C>T | NP_005723.2:p.Asp478= | |
| NM_005732.4:c.1434C>T MANE Select | NP_005723.2:p.Asp478= |