Linked Data
ClinVar Variation Id:
1020537
ClinVar RCV Id:
RCV002543794
dbSNP Id:
rs867184583
gnomAD v3:
16-50699872-T-G
gnomAD v4:
16-50699872-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.50699872T>G , CM000678.2:g.50699872T>G | GRCh38 |
| NC_000016.9:g.50733783T>G , CM000678.1:g.50733783T>G | GRCh37 |
| NC_000016.8:g.49291284T>G | NCBI36 |
| NG_007508.1:g.7734T>G , LRG_177:g.7734T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641284.2:c.377T>G | ENSP00000493088.1:p.Leu126Arg | |
| ENST00000646677.2:c.377T>G | ENSP00000496533.1:p.Leu126Arg | |
| ENST00000641284.1:c.377T>G | ENSP00000493088.1:p.Leu126Arg | |
| ENST00000646677.1:c.377T>G | ENSP00000496533.1:p.Leu126Arg | |
| ENST00000647318.2:c.377T>G MANE Select | ENSP00000495993.1:p.Leu126Arg | |
| ENST00000300589.6:c.458T>G | ENSP00000300589.2:p.Leu153Arg | |
| ENST00000526417.6:n.445T>G | ||
| ENST00000527070.5:c.*1073T>G | ENSP00000435149.1:n.*1073T>G | |
| ENST00000531674.1:c.377T>G | ENSP00000431681.1:p.Leu126Arg | |
| ENST00000532206.1:n.562T>G | ||
| NM_001293557.1:c.377T>G | NP_001280486.1:p.Leu126Arg | |
| NM_022162.2:c.458T>G | NP_071445.1:p.Leu153Arg | |
| XM_005256084.2:c.377T>G | XP_005256141.1:p.Leu126Arg | |
| XM_006721242.2:c.377T>G | XP_006721305.1:p.Leu126Arg | |
| XM_006721243.2:c.377T>G | XP_006721306.1:p.Leu126Arg | |
| XM_011523257.1:c.-120T>G | XP_011521559.1:n.-120T>G | |
| XM_011523258.1:c.-38+6210T>G | XP_011521560.1:n.-38+6210T>G | |
| XM_011523259.1:c.-103T>G | XP_011521561.1:n.-103T>G | |
| XM_011523260.1:c.377T>G | XP_011521562.1:p.Leu126Arg | |
| XM_011523261.1:c.377T>G | XP_011521563.1:p.Leu126Arg | |
| XR_429725.2:n.467T>G | ||
| XR_429726.2:n.467T>G | ||
| XR_933387.1:n.467T>G | ||
| XM_005256084.4:c.377T>G | XP_005256141.1:p.Leu126Arg | |
| XM_006721242.4:c.377T>G | XP_006721305.1:p.Leu126Arg | |
| XM_006721243.4:c.377T>G | XP_006721306.1:p.Leu126Arg | |
| XM_011523259.2:c.-103T>G | XP_011521561.1:n.-103T>G | |
| XM_011523260.3:c.377T>G | XP_011521562.1:p.Leu126Arg | |
| XM_011523261.2:c.377T>G | XP_011521563.1:p.Leu126Arg | |
| XM_017023536.1:c.-127+6210T>G | XP_016879025.1:n.-127+6210T>G | |
| XM_017023537.1:c.-21+6210T>G | XP_016879026.1:n.-21+6210T>G | |
| XR_429725.3:n.420T>G | ||
| XR_429726.3:n.420T>G | ||
| XR_933387.2:n.420T>G | ||
| NM_001293557.2:c.377T>G | NP_001280486.1:p.Leu126Arg | |
| NM_001370466.1:c.377T>G MANE Select | NP_001357395.1:p.Leu126Arg | |
| NM_022162.3:c.458T>G | NP_071445.1:p.Leu153Arg | |
| NR_163434.1:n.442T>G |