Linked Data
ClinVar Variation Id:
478454
dbSNP Id:
rs374290346
ExAC:
3:52360252 T / C
gnomAD v2:
3-52360252-T-C
gnomAD v3:
3-52326236-T-C
gnomAD v4:
3-52326236-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52326236T>C , CM000665.2:g.52326236T>C | GRCh38 |
| NC_000003.11:g.52360252T>C , CM000665.1:g.52360252T>C | GRCh37 |
| NC_000003.10:g.52335292T>C | NCBI36 |
| NG_052911.1:g.14918T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420323.7:c.503T>C MANE Select | ENSP00000401514.2:p.Leu168Pro | |
| ENST00000420323.6:c.503T>C | ENSP00000401514.2:p.Leu168Pro | |
| ENST00000486752.5:n.764T>C | ||
| ENST00000497875.1:n.668T>C | ||
| NM_015512.4:c.503T>C | NP_056327.4:p.Leu168Pro | |
| XM_011533577.1:c.503T>C | XP_011531879.1:p.Leu168Pro | |
| XM_017006129.1:c.503T>C | XP_016861618.1:p.Leu168Pro | |
| XM_017006130.1:c.503T>C | XP_016861619.1:p.Leu168Pro | |
| XM_017006131.1:c.503T>C | XP_016861620.1:p.Leu168Pro | |
| XM_017006132.1:c.503T>C | XP_016861621.1:p.Leu168Pro | |
| XM_017006133.1:c.503T>C | XP_016861622.1:p.Leu168Pro | |
| XR_001740098.1:n.3652T>C | ||
| XR_001740099.1:n.3652T>C | ||
| NM_015512.5:c.503T>C MANE Select | NP_056327.4:p.Leu168Pro |