Linked Data
ClinVar Variation Id:
640832
ClinVar RCV Id:
RCV003535864
dbSNP Id:
rs1580996349
gnomAD v4:
5-112707603-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112707603T>C , CM000667.2:g.112707603T>C | GRCh38 |
| NC_000005.9:g.112043300T>C , CM000667.1:g.112043300T>C | GRCh37 |
| NC_000005.8:g.112071199T>C | NCBI36 |
| NG_008481.4:g.20083T>C , LRG_130:g.20083T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000505350.2:c.-115T>C | ENSP00000481752.1:n.-115T>C | |
| ENST00000507379.6:c.-115T>C | ENSP00000423224.2:n.-115T>C | |
| ENST00000509732.6:c.-65T>C | ENSP00000426541.2:n.-65T>C | |
| ENST00000505350.1:c.-115T>C | ENSP00000481752.1:n.-115T>C | |
| ENST00000507379.5:c.-115T>C | ENSP00000423224.1:n.-115T>C | |
| ENST00000509732.5:c.-65T>C | ENSP00000426541.1:n.-65T>C | |
| NM_001127511.2:c.-115T>C | NP_001120983.2:n.-115T>C | |
| NM_001354895.1:c.-298T>C | NP_001341824.1:n.-298T>C | |
| NM_001354897.1:c.-115T>C | NP_001341826.1:n.-115T>C | |
| NM_001354902.1:c.-115T>C | NP_001341831.1:n.-115T>C | |
| NM_001127511.3:c.-115T>C | NP_001120983.2:n.-115T>C | |
| NM_001354895.2:c.-298T>C | NP_001341824.1:n.-298T>C | |
| NM_001354897.2:c.-115T>C | NP_001341826.1:n.-115T>C | |
| NM_001354902.2:c.-115T>C | NP_001341831.1:n.-115T>C |