Linked Data
ClinVar Variation Id:
2707882
ClinVar RCV Id:
RCV003545080
dbSNP Id:
rs1316644454
gnomAD v3:
4-6301503-C-G
gnomAD v4:
4-6301503-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6301503C>G , CM000666.2:g.6301503C>G | GRCh38 |
| NC_000004.11:g.6303230C>G , CM000666.1:g.6303230C>G | GRCh37 |
| NC_000004.10:g.6354131C>G | NCBI36 |
| NG_011700.1:g.36654C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682275.1:c.1744C>G | ENSP00000507852.1:p.Leu582Val | |
| ENST00000683395.1:c.1685C>G | ||
| ENST00000684087.1:c.1708C>G | ENSP00000506978.1:p.Leu570Val | |
| ENST00000506362.2:c.1459C>G | ENSP00000424103.2:p.Leu487Val | |
| ENST00000673642.1:c.1367C>G | ENSP00000501242.1:n.1367C>G | |
| ENST00000673991.1:c.1744C>G | ENSP00000501033.1:p.Leu582Val | |
| ENST00000226760.5:c.1708C>G MANE Select | ENSP00000226760.1:p.Leu570Val | |
| ENST00000503569.5:c.1708C>G | ENSP00000423337.1:p.Leu570Val | |
| ENST00000507765.1:n.1893C>G | ||
| NM_001145853.1:c.1708C>G | NP_001139325.1:p.Leu570Val | |
| NM_006005.3:c.1708C>G MANE Select | NP_005996.2:p.Leu570Val | |
| XM_017008586.1:c.1717C>G | XP_016864075.1:p.Leu573Val |