Linked Data
ClinVar Variation Id:
1754633
dbSNP Id:
rs140298583
ExAC:
17:42429430 G / T
gnomAD v2:
17-42429430-G-T
gnomAD v3:
17-44352062-G-T
gnomAD v4:
17-44352062-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44352062G>T , CM000679.2:g.44352062G>T | GRCh38 |
| NC_000017.10:g.42429430G>T , CM000679.1:g.42429430G>T | GRCh37 |
| NC_000017.9:g.39784956G>T | NCBI36 |
| NG_007886.1:g.11940G>T , LRG_661:g.11940G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000053867.8:c.1227G>T MANE Select | ENSP00000053867.2:p.Thr409= | |
| ENST00000639447.1:c.1136+310G>T | ENSP00000492014.1:n.1136+310G>T | |
| ENST00000053867.7:c.1227G>T | ENSP00000053867.2:p.Thr409= | |
| ENST00000586443.1:c.668G>T | ||
| ENST00000589265.5:c.756G>T | ENSP00000467616.1:p.Thr252= | |
| NM_002087.3:c.1227G>T | NP_002078.1:p.Thr409= | |
| XM_005257253.1:c.1227G>T | XP_005257310.1:p.Thr409= | |
| XM_024450730.1:c.1227G>T | XP_024306498.1:p.Thr409= | |
| NM_002087.4:c.1227G>T MANE Select | NP_002078.1:p.Thr409= |