Linked Data
ClinVar Variation Id:
21581
dbSNP Id:
rs199422160
ExAC:
1:197091288 C / T
gnomAD v2:
1-197091288-C-T
gnomAD v4:
1-197122158-C-T
PubMed:
PMID:20301772
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197122158C>T , CM000663.2:g.197122158C>T | GRCh38 |
| NC_000001.10:g.197091288C>T , CM000663.1:g.197091288C>T | GRCh37 |
| NC_000001.9:g.195357911C>T | NCBI36 |
| NG_015867.1:g.29537G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367408.6:n.1783+1G>A | ||
| ENST00000367409.9:c.3741+1G>A MANE Select | ENSP00000356379.4:n.3741+1G>A | |
| ENST00000680112.1:n.1797+1G>A | ||
| ENST00000680265.1:c.3741+1G>A | ENSP00000505384.1:n.3741+1G>A | |
| ENST00000680710.1:c.3741+1G>A | ENSP00000506676.1:n.3741+1G>A | |
| ENST00000681879.1:c.3741+1G>A | ENSP00000505363.1:n.3741+1G>A | |
| ENST00000294732.11:c.3741+1G>A | ENSP00000294732.7:n.3741+1G>A | |
| ENST00000367408.5:c.1491+1G>A | ENSP00000356378.1:n.1491+1G>A | |
| ENST00000367409.8:c.3741+1G>A | ENSP00000356379.4:n.3741+1G>A | |
| ENST00000612785.1:c.562-19511G>A | ENSP00000479244.1:n.562-19511G>A | |
| NM_001206846.1:c.3741+1G>A | NP_001193775.1:n.3741+1G>A | |
| NM_018136.4:c.3741+1G>A | NP_060606.3:n.3741+1G>A | |
| NM_018136.5:c.3741+1G>A MANE Select | NP_060606.3:n.3741+1G>A | |
| NM_001206846.2:c.3741+1G>A | NP_001193775.1:n.3741+1G>A |