Linked Data
dbSNP Id:
rs1053701399
gnomAD v2:
10-124231581-C-G
gnomAD v3:
10-122472065-C-G
gnomAD v4:
10-122472065-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122472065C>G , CM000672.2:g.122472065C>G | GRCh38 |
| NC_000010.10:g.124231581C>G , CM000672.1:g.124231581C>G | GRCh37 |
| NC_000010.9:g.124221571C>G | NCBI36 |
| NG_011554.1:g.15541C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.472+9941C>G MANE Select | ENSP00000357980.3:n.472+9941C>G | |
| ENST00000648167.1:c.154+13356C>G | ENSP00000498033.1:n.154+13356C>G | |
| ENST00000368984.7:c.472+9941C>G | ENSP00000357980.3:n.472+9941C>G | |
| NM_002775.4:c.472+9941C>G | NP_002766.1:n.472+9941C>G | |
| NM_002775.5:c.472+9941C>G MANE Select | NP_002766.1:n.472+9941C>G |