Linked Data
ClinVar Variation Id:
2636679
ClinVar RCV Id:
RCV003420980
dbSNP Id:
rs1776226305
gnomAD v3:
6-32040473-C-T
gnomAD v4:
6-32040473-C-T
COSMIC:
COSM3624998
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32040473C>T , CM000668.2:g.32040473C>T | GRCh38 |
| NC_000006.11:g.32008250C>T , CM000668.1:g.32008250C>T | GRCh37 |
| NC_000006.10:g.32116229C>T | NCBI36 |
| NG_007941.2:g.7166C>T | |
| NG_008337.2:g.73902G>A | |
| NG_007941.3:g.7169C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644719.2:c.1007C>T MANE Select | ENSP00000496625.1:p.Pro336Leu | |
| ENST00000418967.6:c.1007C>T | ENSP00000408860.2:p.Pro336Leu | |
| ENST00000435122.3:c.917C>T | ENSP00000415043.2:p.Pro306Leu | |
| ENST00000479074.5:n.1065C>T | ||
| ENST00000479730.5:n.1123C>T | ||
| ENST00000483041.5:n.1176C>T | ||
| ENST00000486063.5:n.986C>T | ||
| NM_000500.7:c.1007C>T | NP_000491.4:p.Pro336Leu | |
| NM_001128590.3:c.917C>T | NP_001122062.3:p.Pro306Leu | |
| XM_011514314.1:c.602C>T | XP_011512616.1:p.Pro201Leu | |
| NM_000500.9:c.1007C>T MANE Select | NP_000491.4:p.Pro336Leu | |
| NM_001368143.1:c.602C>T | NP_001355072.1:p.Pro201Leu | |
| NM_001368144.1:c.602C>T | NP_001355073.1:p.Pro201Leu | |
| NM_001128590.4:c.917C>T | NP_001122062.3:p.Pro306Leu | |
| NM_001368143.2:c.602C>T | NP_001355072.1:p.Pro201Leu | |
| NM_001368144.2:c.602C>T | NP_001355073.1:p.Pro201Leu |