Linked Data
dbSNP Id:
rs145410177
gnomAD v2:
10-79793539-C-G
gnomAD v3:
10-78033781-C-G
gnomAD v4:
10-78033781-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.78033781C>G , CM000672.2:g.78033781C>G | GRCh38 |
| NC_000010.10:g.79793539C>G , CM000672.1:g.79793539C>G | GRCh37 |
| NC_000010.9:g.79463545C>G | NCBI36 |
| NG_012633.1:g.5022C>G | |
| NG_029648.1:g.760G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613865.5:c.-121C>G | ENSP00000478869.2:n.-121C>G | |
| ENST00000435275.5:c.-121C>G | ENSP00000415549.1:n.-121C>G | |
| ENST00000440692.5:c.-121C>G | ENSP00000414321.1:n.-121C>G | |
| ENST00000613865.4:c.-121C>G | ENSP00000478869.1:n.-121C>G | |
| NM_001026.4:c.-121C>G | NP_001017.1:n.-121C>G | |
| NM_001142282.1:c.-121C>G | NP_001135754.1:n.-121C>G | |
| NM_001142283.1:c.-121C>G | NP_001135755.1:n.-121C>G | |
| NM_001142284.1:c.-121C>G | NP_001135756.1:n.-121C>G | |
| NM_001142285.1:c.-121C>G | NP_001135757.1:n.-121C>G | |
| NM_033022.3:c.-121C>G | NP_148982.1:n.-121C>G |