Linked Data
dbSNP Id:
rs370533898
gnomAD v2:
1-153963738-C-T
gnomAD v3:
1-153991262-C-T
gnomAD v4:
1-153991262-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.153991262C>T , CM000663.2:g.153991262C>T | GRCh38 |
| NC_000001.10:g.153963738C>T , CM000663.1:g.153963738C>T | GRCh37 |
| NC_000001.9:g.152230362C>T | NCBI36 |
| NG_053102.2:g.5508C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000477151.2:n.303+39C>T | ||
| ENST00000643794.1:c.236+39C>T | ENSP00000495765.1:n.236+39C>T | |
| ENST00000651669.1:c.115+39C>T MANE Select | ENSP00000499044.1:n.115+39C>T | |
| ENST00000368567.4:c.115+39C>T | ENSP00000357555.4:n.115+39C>T | |
| ENST00000392558.4:c.154C>T | ENSP00000376341.4:p.Pro52Ser | |
| ENST00000477151.1:n.270+39C>T | ||
| ENST00000493224.5:n.381+39C>T | ||
| NM_001030.4:c.115+39C>T | NP_001021.1:n.115+39C>T | |
| NM_001030.6:c.115+39C>T MANE Select | NP_001021.1:n.115+39C>T | |
| NM_001349946.1:c.19+39C>T | NP_001336875.1:n.19+39C>T | |
| NM_001349947.1:c.19+39C>T | NP_001336876.1:n.19+39C>T | |
| NM_001349946.2:c.19+39C>T | NP_001336875.1:n.19+39C>T | |
| NM_001349947.2:c.19+39C>T | NP_001336876.1:n.19+39C>T |