Linked Data
ClinVar Variation Id:
256365
dbSNP Id:
rs139066906
ExAC:
19:11222296 G / A
gnomAD v2:
19-11222296-G-A
gnomAD v3:
19-11111620-G-A
gnomAD v4:
19-11111620-G-A
ERepo:
CA032357/MONDO:0007750/013
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11111620G>A , CM000681.2:g.11111620G>A | GRCh38 |
| NC_000019.9:g.11222296G>A , CM000681.1:g.11222296G>A | GRCh37 |
| NC_000019.8:g.11083296G>A | NCBI36 |
| NG_009060.1:g.27240G>A , LRG_274:g.27240G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000252444.10:c.1425G>A | ENSP00000252444.6:p.Thr475= | |
| ENST00000559340.2:c.1167G>A | ENSP00000453696.2:p.Thr389= | |
| ENST00000560467.2:c.1047G>A | ENSP00000453513.2:p.Thr349= | |
| ENST00000558518.6:c.1167G>A MANE Select | ENSP00000454071.1:p.Thr389= | |
| ENST00000252444.9:c.1421G>A | ||
| ENST00000455727.6:c.663G>A | ENSP00000397829.2:p.Thr221= | |
| ENST00000535915.5:c.1044G>A | ENSP00000440520.1:p.Thr348= | |
| ENST00000545707.5:c.786G>A | ENSP00000437639.1:p.Thr262= | |
| ENST00000557933.5:c.1167G>A | ENSP00000453557.1:p.Thr389= | |
| ENST00000558013.5:c.1167G>A | ENSP00000453346.1:p.Thr389= | |
| ENST00000558518.5:c.1167G>A | ENSP00000454071.1:p.Thr389= | |
| ENST00000560173.1:n.166G>A | ||
| ENST00000560467.1:c.647G>A | ||
| NM_000527.4:c.1167G>A , LRG_274t1:c.1167G>A | NP_000518.1:p.Thr389= | |
| NM_001195798.1:c.1167G>A | NP_001182727.1:p.Thr389= | |
| NM_001195799.1:c.1044G>A | NP_001182728.1:p.Thr348= | |
| NM_001195800.1:c.663G>A | NP_001182729.1:p.Thr221= | |
| NM_001195803.1:c.786G>A | NP_001182732.1:p.Thr262= | |
| XM_011528010.1:c.1167G>A | XP_011526312.1:p.Thr389= | |
| XM_011528011.1:c.786G>A | XP_011526313.1:p.Thr262= | |
| XR_244074.2:n.1317G>A | ||
| XM_011528010.2:c.1167G>A | XP_011526312.1:p.Thr389= | |
| XR_001753685.2:n.1284G>A | ||
| XR_001753686.2:n.1284G>A | ||
| NM_000527.5:c.1167G>A MANE Select | NP_000518.1:p.Thr389= | |
| NM_001195798.2:c.1167G>A | NP_001182727.1:p.Thr389= | |
| NM_001195799.2:c.1044G>A | NP_001182728.1:p.Thr348= | |
| NM_001195800.2:c.663G>A | NP_001182729.1:p.Thr221= | |
| NM_001195803.2:c.786G>A | NP_001182732.1:p.Thr262= |