Linked Data
ClinVar Variation Id:
383002
ClinVar RCV Id:
RCV000870941
dbSNP Id:
rs142629496
ExAC:
11:125472225 C / T
gnomAD v2:
11-125472225-C-T
gnomAD v3:
11-125602330-C-T
gnomAD v4:
11-125602330-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.125602330C>T , CM000673.2:g.125602330C>T | GRCh38 |
| NC_000011.9:g.125472225C>T , CM000673.1:g.125472225C>T | GRCh37 |
| NC_000011.8:g.124977435C>T | NCBI36 |
| NG_042806.1:g.14536C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392708.9:c.177C>T MANE Select | ENSP00000376472.3:p.Phe59= | |
| ENST00000649491.1:c.177C>T | ENSP00000497336.1:p.Phe59= | |
| ENST00000392708.8:c.177C>T | ENSP00000376472.3:p.Phe59= | |
| ENST00000525652.5:c.177C>T | ENSP00000435810.1:p.Phe59= | |
| ENST00000527606.5:c.177C>T | ENSP00000436558.1:p.Phe59= | |
| ENST00000529196.5:c.177C>T | ENSP00000436962.1:p.Phe59= | |
| ENST00000529886.1:c.177C>T | ENSP00000432912.1:p.Phe59= | |
| ENST00000531491.5:c.-100C>T | ENSP00000432820.1:n.-100C>T | |
| ENST00000534472.5:n.312C>T | ||
| NM_001278503.1:c.177C>T | NP_001265432.1:p.Phe59= | |
| NM_001278504.1:c.-100C>T | NP_001265433.1:n.-100C>T | |
| NM_152713.4:c.177C>T | NP_689926.1:p.Phe59= | |
| XM_011542807.1:c.177C>T | XP_011541109.1:p.Phe59= | |
| XM_011542808.1:c.177C>T | XP_011541110.1:p.Phe59= | |
| XM_011542807.3:c.177C>T | XP_011541109.1:p.Phe59= | |
| XR_001747860.2:n.284C>T | ||
| NM_001278503.2:c.177C>T | NP_001265432.1:p.Phe59= | |
| NM_001278504.2:c.-100C>T | NP_001265433.1:n.-100C>T | |
| NM_152713.5:c.177C>T MANE Select | NP_689926.1:p.Phe59= |