Linked Data
dbSNP Id:
rs780466193
ExAC:
12:12871270 T / C
gnomAD v2:
12-12871270-T-C
gnomAD v3:
12-12718336-T-C
gnomAD v4:
12-12718336-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12718336T>C , CM000674.2:g.12718336T>C | GRCh38 |
| NC_000012.11:g.12871270T>C , CM000674.1:g.12871270T>C | GRCh37 |
| NC_000012.10:g.12762537T>C | NCBI36 |
| NG_016341.1:g.5969T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614874.2:c.475+22T>C | ENSP00000507272.1:n.475+22T>C | |
| ENST00000682620.1:n.1631-489T>C | ||
| ENST00000684771.1:n.585-489T>C | ||
| ENST00000228872.9:c.475+22T>C MANE Select | ENSP00000228872.4:n.475+22T>C | |
| ENST00000228872.8:c.475+22T>C | ENSP00000228872.4:n.475+22T>C | |
| ENST00000396340.1:c.475+22T>C | ENSP00000379629.1:n.475+22T>C | |
| ENST00000442489.1:c.193+283T>C | ENSP00000407597.1:n.193+283T>C | |
| ENST00000477087.1:n.155-489T>C | ||
| NM_004064.4:c.475+22T>C | NP_004055.1:n.475+22T>C | |
| NM_004064.5:c.475+22T>C MANE Select | NP_004055.1:n.475+22T>C |