Linked Data
ClinVar Variation Id:
313193
dbSNP Id:
rs77374493
ExAC:
14:45606290 C / T
gnomAD v2:
14-45606290-C-T
gnomAD v3:
14-45137087-C-T
gnomAD v4:
14-45137087-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.45137087C>T , CM000676.2:g.45137087C>T | GRCh38 |
| NC_000014.8:g.45606290C>T , CM000676.1:g.45606290C>T | GRCh37 |
| NC_000014.7:g.44676040C>T | NCBI36 |
| NG_007417.1:g.6155C>T , LRG_502:g.6155C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000554030.2:c.527C>T | ENSP00000512773.1:p.Thr176Ile | |
| ENST00000556036.6:c.527C>T | ENSP00000450596.1:p.Thr176Ile | |
| ENST00000556250.6:c.527C>T | ENSP00000452033.2:p.Thr176Ile | |
| ENST00000696641.1:c.527C>T | ENSP00000512774.1:p.Thr176Ile | |
| ENST00000696642.1:c.527C>T | ENSP00000512775.1:p.Thr176Ile | |
| ENST00000696643.1:c.527C>T | ENSP00000512776.1:p.Thr176Ile | |
| ENST00000696646.1:c.527C>T | ENSP00000512777.1:p.Thr176Ile | |
| ENST00000696647.1:c.527C>T | ENSP00000512778.1:p.Thr176Ile | |
| ENST00000696648.1:c.527C>T | ENSP00000512779.1:p.Thr176Ile | |
| ENST00000696649.1:c.527C>T | ENSP00000512780.1:p.Thr176Ile | |
| ENST00000696650.1:n.553C>T | ||
| ENST00000696656.1:n.556C>T | ||
| ENST00000696657.1:c.508+548C>T | ENSP00000512784.1:n.508+548C>T | |
| ENST00000696658.1:n.1077C>T | ||
| ENST00000696662.1:c.527C>T | ENSP00000512788.1:p.Thr176Ile | |
| ENST00000696675.1:c.527C>T | ENSP00000512799.1:p.Thr176Ile | |
| ENST00000696676.1:c.487C>T | ENSP00000512800.1:p.Pro163Ser | |
| ENST00000696677.1:c.487C>T | ENSP00000512801.1:p.Pro163Ser | |
| ENST00000696678.1:n.556C>T | ||
| ENST00000696679.1:c.508+548C>T | ENSP00000512802.1:n.508+548C>T | |
| ENST00000696680.1:c.527C>T | ENSP00000512803.1:p.Thr176Ile | |
| ENST00000696681.1:c.527C>T | ENSP00000512804.1:p.Thr176Ile | |
| ENST00000696682.1:c.527C>T | ENSP00000512805.1:p.Thr176Ile | |
| ENST00000267430.10:c.527C>T MANE Select | ENSP00000267430.5:p.Thr176Ile | |
| ENST00000267430.9:c.527C>T | ENSP00000267430.5:p.Thr176Ile | |
| ENST00000542564.6:c.527C>T | ENSP00000442493.2:p.Thr176Ile | |
| ENST00000554030.1:n.45C>T | ||
| ENST00000556036.5:c.527C>T | ENSP00000450596.1:p.Thr176Ile | |
| NM_001308133.1:c.527C>T | NP_001295062.1:p.Thr176Ile | |
| NM_001308134.1:c.527C>T | NP_001295063.1:p.Thr176Ile | |
| NM_020937.2:c.527C>T , LRG_502t1:c.527C>T | NP_065988.1:p.Thr176Ile | |
| NM_020937.3:c.527C>T | NP_065988.1:p.Thr176Ile | |
| XM_011537034.1:c.527C>T | XP_011535336.1:p.Thr176Ile | |
| XM_011537035.1:c.527C>T | XP_011535337.1:p.Thr176Ile | |
| XM_011537036.1:c.527C>T | XP_011535338.1:p.Thr176Ile | |
| XM_011537034.2:c.527C>T | XP_011535336.1:p.Thr176Ile | |
| XM_011537035.3:c.527C>T | XP_011535337.1:p.Thr176Ile | |
| XM_017021523.1:c.527C>T | XP_016877012.1:p.Thr176Ile | |
| XM_017021524.2:c.-205+548C>T | XP_016877013.1:n.-205+548C>T | |
| XM_017021525.2:c.-448C>T | XP_016877014.1:n.-448C>T | |
| XM_017021527.1:c.-526C>T | XP_016877016.1:n.-526C>T | |
| XR_001750470.1:n.619C>T | ||
| XR_001750471.2:n.619C>T | ||
| XR_001750472.1:n.619C>T | ||
| NM_020937.4:c.527C>T MANE Select | NP_065988.1:p.Thr176Ile | |
| NM_001308133.2:c.527C>T | NP_001295062.1:p.Thr176Ile | |
| NM_001308134.2:c.527C>T | NP_001295063.1:p.Thr176Ile |