Linked Data
ClinVar Variation Id:
1010469
dbSNP Id:
rs146588560
ExAC:
4:997403 G / T
gnomAD v2:
4-997403-G-T
gnomAD v3:
4-1003615-G-T
gnomAD v4:
4-1003615-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.1003615G>T , CM000666.2:g.1003615G>T | GRCh38 |
| NC_000004.11:g.997403G>T , CM000666.1:g.997403G>T | GRCh37 |
| NC_000004.10:g.987403G>T | NCBI36 |
| NG_008103.1:g.21619G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000247933.9:c.1717G>T | ENSP00000247933.4:p.Val573Leu | |
| ENST00000514224.2:c.1717G>T MANE Select | ENSP00000425081.2:p.Val573Leu | |
| ENST00000652070.1:n.1773G>T | ||
| ENST00000247933.8:c.1717G>T | ENSP00000247933.4:p.Val573Leu | |
| ENST00000514224.1:c.1321G>T | ENSP00000425081.1:p.Val441Leu | |
| ENST00000514417.1:n.109G>T | ||
| ENST00000514698.5:n.1824G>T | ||
| NM_000203.4:c.1717G>T | NP_000194.2:p.Val573Leu | |
| NR_110313.1:n.1805G>T | ||
| XM_006713882.2:c.1321G>T | XP_006713945.1:p.Val441Leu | |
| XM_011513459.1:c.1783G>T | XP_011511761.1:p.Val595Leu | |
| XM_011513460.1:c.1576G>T | XP_011511762.1:p.Val526Leu | |
| XM_011513461.1:c.1510G>T | XP_011511763.1:p.Val504Leu | |
| XM_011513462.1:c.1429G>T | XP_011511764.1:p.Val477Leu | |
| XM_011513463.1:c.1429G>T | XP_011511765.1:p.Val477Leu | |
| XR_924947.1:n.1973G>T | ||
| NM_000203.5:c.1717G>T MANE Select | NP_000194.2:p.Val573Leu | |
| NM_001363576.1:c.1321G>T | NP_001350505.1:p.Val441Leu | |
| XM_011513461.2:c.1510G>T | XP_011511763.1:p.Val504Leu | |
| XM_017008163.1:c.757G>T | XP_016863652.1:p.Val253Leu |