Linked Data
ClinVar Variation Id:
1104377
ClinVar RCV Id:
RCV001428422
dbSNP Id:
rs1431449120
gnomAD v3:
12-12718323-C-T
gnomAD v4:
12-12718323-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12718323C>T , CM000674.2:g.12718323C>T | GRCh38 |
| NC_000012.11:g.12871257C>T , CM000674.1:g.12871257C>T | GRCh37 |
| NC_000012.10:g.12762524C>T | NCBI36 |
| NG_016341.1:g.5956C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614874.2:c.475+9C>T | ENSP00000507272.1:n.475+9C>T | |
| ENST00000682620.1:n.1631-502C>T | ||
| ENST00000684771.1:n.585-502C>T | ||
| ENST00000228872.9:c.475+9C>T MANE Select | ENSP00000228872.4:n.475+9C>T | |
| ENST00000228872.8:c.475+9C>T | ENSP00000228872.4:n.475+9C>T | |
| ENST00000396340.1:c.475+9C>T | ENSP00000379629.1:n.475+9C>T | |
| ENST00000442489.1:c.193+270C>T | ENSP00000407597.1:n.193+270C>T | |
| ENST00000477087.1:n.155-502C>T | ||
| NM_004064.4:c.475+9C>T | NP_004055.1:n.475+9C>T | |
| NM_004064.5:c.475+9C>T MANE Select | NP_004055.1:n.475+9C>T |