Linked Data
ClinVar Variation Id:
520117
dbSNP Id:
rs1401035675
gnomAD v3:
1-11965478-A-G
gnomAD v4:
1-11965478-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11965478A>G , CM000663.2:g.11965478A>G | GRCh38 |
| NC_000001.10:g.12025535A>G , CM000663.1:g.12025535A>G | GRCh37 |
| NC_000001.9:g.11948122A>G | NCBI36 |
| NG_008159.1:g.35790A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000196061.5:c.1471-2A>G MANE Select | ENSP00000196061.4:n.1471-2A>G | |
| ENST00000196061.4:c.1471-2A>G | ENSP00000196061.4:n.1471-2A>G | |
| ENST00000470133.1:n.85-2A>G | ||
| ENST00000491536.5:n.99-2A>G | ||
| NM_000302.3:c.1471-2A>G | NP_000293.2:n.1471-2A>G | |
| NM_001316320.1:c.1612-2A>G | NP_001303249.1:n.1612-2A>G | |
| XM_011541594.1:c.1552-2A>G | XP_011539896.1:n.1552-2A>G | |
| XM_024447707.1:c.805-2A>G | XP_024303475.1:n.805-2A>G | |
| NM_000302.4:c.1471-2A>G MANE Select | NP_000293.2:n.1471-2A>G | |
| NM_001316320.2:c.1612-2A>G | NP_001303249.1:n.1612-2A>G |