Linked Data
dbSNP Id:
rs1299056901
gnomAD v2:
6-32006321-T-C
gnomAD v3:
6-32038544-T-C
gnomAD v4:
6-32038544-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32038544T>C , CM000668.2:g.32038544T>C | GRCh38 |
| NC_000006.11:g.32006321T>C , CM000668.1:g.32006321T>C | GRCh37 |
| NC_000006.10:g.32114300T>C | NCBI36 |
| NG_007941.2:g.5237T>C | |
| NG_007941.3:g.5240T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644719.2:c.122T>C MANE Select | ENSP00000496625.1:p.Leu41Pro | |
| ENST00000418967.6:c.122T>C | ENSP00000408860.2:p.Leu41Pro | |
| ENST00000435122.3:c.122T>C | ENSP00000415043.2:p.Leu41Pro | |
| ENST00000466779.5:c.122T>C | ENSP00000417321.1:p.Leu41Pro | |
| ENST00000469053.5:c.122T>C | ENSP00000418104.1:p.Leu41Pro | |
| ENST00000471671.4:c.122T>C | ENSP00000418561.1:p.Leu41Pro | |
| ENST00000478281.5:c.122T>C | ENSP00000419572.1:p.Leu41Pro | |
| ENST00000479074.5:n.180T>C | ||
| ENST00000479730.5:n.180T>C | ||
| ENST00000480027.1:n.175T>C | ||
| ENST00000483041.5:n.175T>C | ||
| ENST00000486063.5:n.205T>C | ||
| ENST00000488465.1:n.130T>C | ||
| NM_000500.7:c.122T>C | NP_000491.4:p.Leu41Pro | |
| NM_001128590.3:c.122T>C | NP_001122062.3:p.Leu41Pro | |
| XM_011514314.1:c.-303T>C | XP_011512616.1:n.-303T>C | |
| NM_000500.9:c.122T>C MANE Select | NP_000491.4:p.Leu41Pro | |
| NM_001368143.1:c.-303T>C | NP_001355072.1:n.-303T>C | |
| NM_001368144.1:c.-213T>C | NP_001355073.1:n.-213T>C | |
| NM_001128590.4:c.122T>C | NP_001122062.3:p.Leu41Pro | |
| NM_001368143.2:c.-303T>C | NP_001355072.1:n.-303T>C | |
| NM_001368144.2:c.-213T>C | NP_001355073.1:n.-213T>C |