Linked Data
ClinVar Variation Id:
97450
dbSNP Id:
rs104895199
ExAC:
16:3297065 A / G
gnomAD v2:
16-3297065-A-G
gnomAD v4:
16-3247065-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3247065A>G , CM000678.2:g.3247065A>G | GRCh38 |
| NC_000016.9:g.3297065A>G , CM000678.1:g.3297065A>G | GRCh37 |
| NC_000016.8:g.3237066A>G | NCBI36 |
| NG_007871.1:g.14563T>C , LRG_190:g.14563T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000219596.6:c.1538T>C MANE Select | ENSP00000219596.1:p.Ile513Thr | |
| ENST00000219596.5:c.1538T>C | ENSP00000219596.1:p.Ile513Thr | |
| ENST00000339854.8:c.998T>C | ENSP00000339639.4:p.Ile333Thr | |
| ENST00000536379.5:c.905T>C | ENSP00000445079.1:p.Ile302Thr | |
| ENST00000536980.5:c.905T>C | ENSP00000444178.1:p.Ile302Thr | |
| ENST00000537682.5:c.1538T>C | ENSP00000438611.1:p.Ile513Thr | |
| ENST00000538326.5:c.*163T>C | ENSP00000437486.1:n.*163T>C | |
| ENST00000539145.5:c.459T>C | ENSP00000444471.1:n.459T>C | |
| ENST00000539154.1:n.903T>C | ||
| ENST00000541159.5:c.905T>C | ENSP00000438711.1:p.Ile302Thr | |
| ENST00000542898.5:c.1631T>C | ENSP00000444615.1:p.Ile544Thr | |
| ENST00000570511.5:c.1092T>C | ENSP00000458312.1:n.1092T>C | |
| ENST00000572244.5:c.278-518T>C | ENSP00000461186.1:n.278-518T>C | |
| ENST00000574583.5:c.459T>C | ENSP00000460269.1:n.459T>C | |
| ENST00000576315.5:c.459T>C | ENSP00000460551.1:n.459T>C | |
| ENST00000621655.1:c.905T>C | ENSP00000481436.1:p.Ile302Thr | |
| NM_000243.2:c.1538T>C , LRG_190t1:c.1538T>C | NP_000234.1:p.Ile513Thr | |
| NM_001198536.1:c.905T>C | NP_001185465.1:p.Ile302Thr | |
| XM_017023236.2:c.1535T>C | XP_016878725.1:p.Ile512Thr | |
| XR_001751903.1:n.1727T>C | ||
| NM_000243.3:c.1538T>C MANE Select | NP_000234.1:p.Ile513Thr | |
| NM_001198536.2:c.905T>C | NP_001185465.2:p.Ile302Thr |