Linked Data
ClinVar Variation Id:
1731057
ClinVar RCV Id:
RCV002452066
gnomAD v4:
12-12717872-T-C
MyVariant Identifiers:
chr12:g.12870806T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717872T>C , CM000674.2:g.12717872T>C | GRCh38 |
| NC_000012.11:g.12870806T>C , CM000674.1:g.12870806T>C | GRCh37 |
| NC_000012.10:g.12762073T>C | NCBI36 |
| NG_016341.1:g.5505T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614874.2:c.33T>C | ENSP00000507272.1:p.Pro11= | |
| ENST00000682620.1:n.1631-953T>C | ||
| ENST00000684771.1:n.585-953T>C | ||
| ENST00000228872.9:c.33T>C MANE Select | ENSP00000228872.4:p.Pro11= | |
| ENST00000228872.8:c.33T>C | ENSP00000228872.4:p.Pro11= | |
| ENST00000396340.1:c.33T>C | ENSP00000379629.1:p.Pro11= | |
| ENST00000442489.1:c.12T>C | ENSP00000407597.1:p.Pro4= | |
| ENST00000477087.1:n.155-953T>C | ||
| NM_004064.4:c.33T>C | NP_004055.1:p.Pro11= | |
| NM_004064.5:c.33T>C MANE Select | NP_004055.1:p.Pro11= |