Linked Data
ClinVar Variation Id:
733877
dbSNP Id:
rs140451005
ExAC:
1:116206362 C / T
gnomAD v2:
1-116206362-C-T
gnomAD v3:
1-115663741-C-T
gnomAD v4:
1-115663741-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115663741C>T , CM000663.2:g.115663741C>T | GRCh38 |
| NC_000001.10:g.116206362C>T , CM000663.1:g.116206362C>T | GRCh37 |
| NC_000001.9:g.116007885C>T | NCBI36 |
| NG_016548.1:g.26789C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355485.7:c.285C>T MANE Select | ENSP00000347672.2:p.Ile95= | |
| ENST00000310260.7:c.285C>T | ENSP00000310800.3:p.Ile95= | |
| ENST00000355485.6:c.285C>T | ENSP00000347672.2:p.Ile95= | |
| ENST00000369509.1:c.285C>T | ENSP00000358522.1:p.Ile95= | |
| ENST00000369510.8:c.279C>T | ENSP00000358523.3:p.Ile93= | |
| NM_001172411.1:c.279C>T | NP_001165882.1:p.Ile93= | |
| NM_001172412.1:c.285C>T | NP_001165883.1:p.Ile95= | |
| NM_138959.2:c.285C>T | NP_620409.1:p.Ile95= | |
| NM_138959.3:c.285C>T MANE Select | NP_620409.1:p.Ile95= | |
| NM_001172411.2:c.279C>T | NP_001165882.1:p.Ile93= | |
| NM_001172412.2:c.285C>T | NP_001165883.1:p.Ile95= |