Linked Data
ClinVar Variation Id:
1742721
ClinVar RCV Id:
RCV002335471
dbSNP Id:
rs756647439
ExAC:
2:215645415 G / T
gnomAD v2:
2-215645415-G-T
gnomAD v4:
2-214780691-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214780691G>T , CM000664.2:g.214780691G>T | GRCh38 |
| NC_000002.11:g.215645415G>T , CM000664.1:g.215645415G>T | GRCh37 |
| NC_000002.10:g.215353660G>T | NCBI36 |
| NG_012047.2:g.34014C>A | |
| NG_012047.3:g.34021C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260947.9:c.1183C>A MANE Select | ENSP00000260947.4:p.Pro395Thr | |
| ENST00000421162.2:c.215+16370C>A | ENSP00000392245.2:n.215+16370C>A | |
| ENST00000613192.2:c.158+28721C>A | ENSP00000483275.2:n.158+28721C>A | |
| ENST00000613374.5:c.159-28136C>A | ENSP00000484464.1:n.159-28136C>A | |
| ENST00000613706.5:c.906+277C>A | ENSP00000484976.2:n.906+277C>A | |
| ENST00000617164.5:c.1126C>A | ENSP00000480470.1:p.Pro376Thr | |
| ENST00000619009.5:c.364+11606C>A | ENSP00000482293.1:n.364+11606C>A | |
| ENST00000650978.1:c.1025C>A | ||
| ENST00000260947.8:c.1183C>A | ENSP00000260947.4:p.Pro395Thr | |
| ENST00000421162.1:c.215+16370C>A | ENSP00000392245.1:n.215+16370C>A | |
| ENST00000455743.5:c.*803C>A | ENSP00000412186.1:n.*803C>A | |
| ENST00000613192.1:c.73+28721C>A | ENSP00000483275.1:n.73+28721C>A | |
| ENST00000613374.4:c.159-28136C>A | ENSP00000484464.1:n.159-28136C>A | |
| ENST00000613706.4:c.215+16370C>A | ENSP00000484976.1:n.215+16370C>A | |
| ENST00000617164.4:c.1126C>A | ENSP00000480470.1:p.Pro376Thr | |
| ENST00000619009.4:c.364+11606C>A | ENSP00000482293.1:n.364+11606C>A | |
| ENST00000620057.4:c.365-11379C>A | ENSP00000481988.1:n.365-11379C>A | |
| NM_000465.3:c.1183C>A | NP_000456.2:p.Pro395Thr | |
| NM_001282543.1:c.1126C>A | NP_001269472.1:p.Pro376Thr | |
| NM_001282545.1:c.215+16370C>A | NP_001269474.1:n.215+16370C>A | |
| NM_001282548.1:c.159-28136C>A | NP_001269477.1:n.159-28136C>A | |
| NM_001282549.1:c.364+11606C>A | NP_001269478.1:n.364+11606C>A | |
| NR_104212.1:n.1176C>A | ||
| NR_104215.1:n.1119C>A | ||
| NR_104216.1:n.507-11379C>A | ||
| XM_011511567.1:c.1129C>A | XP_011509869.1:p.Pro377Thr | |
| XM_011511568.1:c.1183C>A | XP_011509870.1:p.Pro395Thr | |
| XM_017004613.1:c.1282C>A | XP_016860102.1:p.Pro428Thr | |
| XM_017004614.1:c.1282C>A | XP_016860103.1:p.Pro428Thr | |
| XR_002959322.1:n.1373C>A | ||
| NM_000465.4:c.1183C>A MANE Select | NP_000456.2:p.Pro395Thr | |
| NM_001282543.2:c.1126C>A | NP_001269472.1:p.Pro376Thr | |
| NM_001282545.2:c.215+16370C>A | NP_001269474.1:n.215+16370C>A | |
| NM_001282548.2:c.159-28136C>A | NP_001269477.1:n.159-28136C>A | |
| NM_001282549.2:c.364+11606C>A | NP_001269478.1:n.364+11606C>A | |
| NR_104212.2:n.1148C>A | ||
| NR_104215.2:n.1091C>A | ||
| NR_104216.2:n.479-11379C>A |