Linked Data
ClinVar Variation Id:
2857591
ClinVar RCV Id:
RCV003621406
gnomAD v4:
12-12718286-A-G
MyVariant Identifiers:
chr12:g.12871220A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12718286A>G , CM000674.2:g.12718286A>G | GRCh38 |
| NC_000012.11:g.12871220A>G , CM000674.1:g.12871220A>G | GRCh37 |
| NC_000012.10:g.12762487A>G | NCBI36 |
| NG_016341.1:g.5919A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614874.2:c.447A>G | ENSP00000507272.1:p.Ala149= | |
| ENST00000682620.1:n.1631-539A>G | ||
| ENST00000684771.1:n.585-539A>G | ||
| ENST00000228872.9:c.447A>G MANE Select | ENSP00000228872.4:p.Ala149= | |
| ENST00000228872.8:c.447A>G | ENSP00000228872.4:p.Ala149= | |
| ENST00000396340.1:c.447A>G | ENSP00000379629.1:p.Ala149= | |
| ENST00000442489.1:c.193+233A>G | ENSP00000407597.1:n.193+233A>G | |
| ENST00000477087.1:n.155-539A>G | ||
| NM_004064.4:c.447A>G | NP_004055.1:p.Ala149= | |
| NM_004064.5:c.447A>G MANE Select | NP_004055.1:p.Ala149= |