Linked Data
ClinVar Variation Id:
1550277
ClinVar RCV Id:
RCV002189622
dbSNP Id:
rs1434427246
gnomAD v2:
3-183853302-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184135514A>G , CM000665.2:g.184135514A>G | GRCh38 |
| NC_000003.11:g.183853302A>G , CM000665.1:g.183853302A>G | GRCh37 |
| NC_000003.10:g.185335996A>G | NCBI36 |
| NG_015826.1:g.5493A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432569.2:c.129A>G | ENSP00000414775.1:p.Leu43= | |
| ENST00000465218.3:n.152A>G | ||
| ENST00000468748.7:n.112A>G | ||
| ENST00000471832.2:c.129A>G | ENSP00000497786.1:p.Leu43= | |
| ENST00000492226.2:n.126A>G | ||
| ENST00000647636.1:c.129A>G | ENSP00000497505.1:p.Leu43= | |
| ENST00000647909.1:c.129A>G | ENSP00000498164.1:p.Leu43= | |
| ENST00000648256.1:c.78A>G | ENSP00000497356.1:p.Leu26= | |
| ENST00000648314.1:c.129A>G | ENSP00000496920.1:p.Leu43= | |
| ENST00000648599.1:c.129A>G | ENSP00000497159.1:p.Leu43= | |
| ENST00000648630.1:c.123A>G | ENSP00000497887.1:p.Leu41= | |
| ENST00000648682.1:c.129A>G | ENSP00000498185.1:p.Leu43= | |
| ENST00000648882.1:c.129A>G | ENSP00000497603.1:p.Leu43= | |
| ENST00000648890.1:c.129A>G | ENSP00000497503.1:p.Leu43= | |
| ENST00000648915.2:c.129A>G MANE Select | ENSP00000497160.1:p.Leu43= | |
| ENST00000649688.1:c.129A>G | ENSP00000497097.1:p.Leu43= | |
| ENST00000649814.1:n.178A>G | ||
| ENST00000650244.1:c.21A>G | ENSP00000497227.1:p.Leu7= | |
| ENST00000273783.7:c.129A>G | ENSP00000273783.3:p.Leu43= | |
| ENST00000432569.1:c.129A>G | ENSP00000414775.1:p.Leu43= | |
| ENST00000432982.5:c.115A>G | ||
| ENST00000444495.1:c.129A>G | ENSP00000409142.1:p.Leu43= | |
| ENST00000481054.5:n.130A>G | ||
| ENST00000491144.5:n.477A>G | ||
| NM_003907.2:c.129A>G | NP_003898.2:p.Leu43= | |
| XR_924208.1:n.1080A>G | ||
| NM_003907.3:c.129A>G MANE Select | NP_003898.2:p.Leu43= | |
| XM_011513266.3:c.-773A>G | XP_011511568.1:n.-773A>G | |
| XR_001740352.2:n.492A>G | ||
| XR_001740353.2:n.492A>G | ||
| XR_924208.2:n.492A>G |