Linked Data
ClinVar Variation Id:
142156
dbSNP Id:
rs144856889
ExAC:
2:215657039 G / A
gnomAD v2:
2-215657039-G-A
gnomAD v3:
2-214792315-G-A
gnomAD v4:
2-214792315-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214792315G>A , CM000664.2:g.214792315G>A | GRCh38 |
| NC_000002.11:g.215657039G>A , CM000664.1:g.215657039G>A | GRCh37 |
| NC_000002.10:g.215365284G>A | NCBI36 |
| NG_012047.2:g.22390C>T | |
| NG_012047.3:g.22397C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260947.9:c.346C>T MANE Select | ENSP00000260947.4:p.His116Tyr | |
| ENST00000421162.2:c.215+4746C>T | ENSP00000392245.2:n.215+4746C>T | |
| ENST00000613192.2:c.158+17097C>T | ENSP00000483275.2:n.158+17097C>T | |
| ENST00000613374.5:c.158+17097C>T | ENSP00000484464.1:n.158+17097C>T | |
| ENST00000613706.5:c.346C>T | ENSP00000484976.2:p.His116Tyr | |
| ENST00000617164.5:c.289C>T | ENSP00000480470.1:p.His97Tyr | |
| ENST00000619009.5:c.346C>T | ENSP00000482293.1:p.His116Tyr | |
| ENST00000650978.1:c.188C>T | ||
| ENST00000260947.8:c.346C>T | ENSP00000260947.4:p.His116Tyr | |
| ENST00000421162.1:c.215+4746C>T | ENSP00000392245.1:n.215+4746C>T | |
| ENST00000455743.5:c.215+4746C>T | ENSP00000412186.1:n.215+4746C>T | |
| ENST00000471787.1:n.260-10806C>T | ||
| ENST00000613192.1:c.73+17097C>T | ENSP00000483275.1:n.73+17097C>T | |
| ENST00000613374.4:c.158+17097C>T | ENSP00000484464.1:n.158+17097C>T | |
| ENST00000613706.4:c.215+4746C>T | ENSP00000484976.1:n.215+4746C>T | |
| ENST00000617164.4:c.289C>T | ENSP00000480470.1:p.His97Tyr | |
| ENST00000619009.4:c.346C>T | ENSP00000482293.1:p.His116Tyr | |
| ENST00000620057.4:c.346C>T | ENSP00000481988.1:p.His116Tyr | |
| NM_000465.3:c.346C>T | NP_000456.2:p.His116Tyr | |
| NM_001282543.1:c.289C>T | NP_001269472.1:p.His97Tyr | |
| NM_001282545.1:c.215+4746C>T | NP_001269474.1:n.215+4746C>T | |
| NM_001282548.1:c.158+17097C>T | NP_001269477.1:n.158+17097C>T | |
| NM_001282549.1:c.346C>T | NP_001269478.1:p.His116Tyr | |
| NR_104212.1:n.357+4746C>T | ||
| NR_104215.1:n.301-10806C>T | ||
| NR_104216.1:n.488C>T | ||
| XM_011511567.1:c.292C>T | XP_011509869.1:p.His98Tyr | |
| XM_011511568.1:c.346C>T | XP_011509870.1:p.His116Tyr | |
| XM_017004613.1:c.445C>T | XP_016860102.1:p.His149Tyr | |
| XM_017004614.1:c.445C>T | XP_016860103.1:p.His149Tyr | |
| XR_002959322.1:n.536C>T | ||
| NM_000465.4:c.346C>T MANE Select | NP_000456.2:p.His116Tyr | |
| NM_001282543.2:c.289C>T | NP_001269472.1:p.His97Tyr | |
| NM_001282545.2:c.215+4746C>T | NP_001269474.1:n.215+4746C>T | |
| NM_001282548.2:c.158+17097C>T | NP_001269477.1:n.158+17097C>T | |
| NM_001282549.2:c.346C>T | NP_001269478.1:p.His116Tyr | |
| NR_104212.2:n.329+4746C>T | ||
| NR_104215.2:n.273-10806C>T | ||
| NR_104216.2:n.460C>T |