Linked Data
dbSNP Id:
rs753480360
ExAC:
20:21117153 T / C
gnomAD v2:
20-21117153-T-C
gnomAD v3:
20-21136512-T-C
gnomAD v4:
20-21136512-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.21136512T>C , CM000682.2:g.21136512T>C | GRCh38 |
| NC_000020.10:g.21117153T>C , CM000682.1:g.21117153T>C | GRCh37 |
| NC_000020.9:g.21065153T>C | NCBI36 |
| NG_033122.1:g.15530T>C | |
| NG_033122.2:g.15533T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619189.5:c.275T>C MANE Select | ENSP00000479542.1:p.Val92Ala | |
| ENST00000611685.4:c.167-9053T>C | ||
| ENST00000616848.4:c.6+4353T>C | ENSP00000480612.1:n.6+4353T>C | |
| ENST00000619189.4:c.275T>C | ENSP00000479542.1:p.Val92Ala | |
| ENST00000619574.4:c.169-9053T>C | ENSP00000484706.1:n.169-9053T>C | |
| ENST00000620553.2:n.331T>C | ||
| ENST00000620891.4:c.6+4353T>C | ENSP00000478019.1:n.6+4353T>C | |
| NM_001163022.1:c.6+4353T>C | NP_001156494.1:n.6+4353T>C | |
| NM_001163023.1:c.6+4353T>C | NP_001156495.1:n.6+4353T>C | |
| NM_001276389.1:c.169-9053T>C | NP_001263318.1:n.169-9053T>C | |
| NM_018474.4:c.275T>C | NP_060944.3:p.Val92Ala | |
| XM_011529296.1:c.275T>C | XP_011527598.1:p.Val92Ala | |
| XM_011529297.1:c.275T>C | XP_011527599.1:p.Val92Ala | |
| XM_011529298.1:c.275T>C | XP_011527600.1:p.Val92Ala | |
| XM_011529299.1:c.6+4353T>C | XP_011527601.1:n.6+4353T>C | |
| XR_937105.1:n.399T>C | ||
| NM_001163022.2:c.6+4353T>C | NP_001156494.1:n.6+4353T>C | |
| NM_001163023.2:c.6+4353T>C | NP_001156495.1:n.6+4353T>C | |
| NM_001276389.2:c.169-9053T>C | NP_001263318.1:n.169-9053T>C | |
| NM_001352434.1:c.275T>C | NP_001339363.1:p.Val92Ala | |
| NM_001352435.1:c.6+4353T>C | NP_001339364.1:n.6+4353T>C | |
| NM_001352436.1:c.-112T>C | NP_001339365.1:n.-112T>C | |
| NM_018474.5:c.275T>C | NP_060944.3:p.Val92Ala | |
| XM_011529296.3:c.275T>C | XP_011527598.1:p.Val92Ala | |
| XM_011529297.3:c.275T>C | XP_011527599.1:p.Val92Ala | |
| XM_011529299.3:c.6+4353T>C | XP_011527601.1:n.6+4353T>C | |
| XM_017027951.2:c.-112T>C | XP_016883440.1:n.-112T>C | |
| XM_017027952.2:c.6+4353T>C | XP_016883441.1:n.6+4353T>C | |
| XR_001754334.2:n.341T>C | ||
| XR_937105.3:n.341T>C | ||
| NM_018474.6:c.275T>C MANE Select | NP_060944.3:p.Val92Ala | |
| NM_001163022.3:c.6+4353T>C | NP_001156494.1:n.6+4353T>C | |
| NM_001163023.3:c.6+4353T>C | NP_001156495.1:n.6+4353T>C | |
| NM_001352434.2:c.275T>C | NP_001339363.1:p.Val92Ala | |
| NM_001352435.2:c.6+4353T>C | NP_001339364.1:n.6+4353T>C | |
| NM_001352436.2:c.-112T>C | NP_001339365.1:n.-112T>C |