Linked Data
ClinVar Variation Id:
1079630
dbSNP Id:
rs1427650079
gnomAD v4:
12-12717902-G-T
MyVariant Identifiers:
chr12:g.12870836G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717902G>T , CM000674.2:g.12717902G>T | GRCh38 |
| NC_000012.11:g.12870836G>T , CM000674.1:g.12870836G>T | GRCh37 |
| NC_000012.10:g.12762103G>T | NCBI36 |
| NG_016341.1:g.5535G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614874.2:c.63G>T | ENSP00000507272.1:p.Ala21= | |
| ENST00000682620.1:n.1631-923G>T | ||
| ENST00000684771.1:n.585-923G>T | ||
| ENST00000228872.9:c.63G>T MANE Select | ENSP00000228872.4:p.Ala21= | |
| ENST00000228872.8:c.63G>T | ENSP00000228872.4:p.Ala21= | |
| ENST00000396340.1:c.63G>T | ENSP00000379629.1:p.Ala21= | |
| ENST00000442489.1:c.42G>T | ENSP00000407597.1:p.Ala14= | |
| ENST00000477087.1:n.155-923G>T | ||
| NM_004064.4:c.63G>T | NP_004055.1:p.Ala21= | |
| NM_004064.5:c.63G>T MANE Select | NP_004055.1:p.Ala21= |