Linked Data
ClinVar Variation Id:
1566
dbSNP Id:
rs104894595
ExAC:
17:40695586 C / T
gnomAD v2:
17-40695586-C-T
gnomAD v3:
17-42543568-C-T
gnomAD v4:
17-42543568-C-T
PubMed:
PMID:10094189
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42543568C>T , CM000679.2:g.42543568C>T | GRCh38 |
| NC_000017.10:g.40695586C>T , CM000679.1:g.40695586C>T | GRCh37 |
| NC_000017.9:g.37949112C>T | NCBI36 |
| NG_011552.1:g.12636C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.1562C>T MANE Select | ENSP00000225927.1:p.Pro521Leu | |
| ENST00000225927.6:c.1562C>T | ENSP00000225927.1:p.Pro521Leu | |
| ENST00000591587.1:c.900C>T | ENSP00000467836.1:n.900C>T | |
| NM_000263.3:c.1562C>T | NP_000254.2:p.Pro521Leu | |
| XM_006721920.2:c.731C>T | XP_006721983.1:p.Pro244Leu | |
| XM_011524840.1:c.563C>T | XP_011523142.1:p.Pro188Leu | |
| XM_017024687.1:c.731C>T | XP_016880176.1:p.Pro244Leu | |
| XM_024450771.1:c.1619C>T | XP_024306539.1:p.Pro540Leu | |
| XM_024450772.1:c.563C>T | XP_024306540.1:p.Pro188Leu | |
| NM_000263.4:c.1562C>T MANE Select | NP_000254.2:p.Pro521Leu |