Linked Data
ClinVar Variation Id:
141977
ClinVar RCV Id:
RCV000130733
RCV000198345
RCV000515236
RCV000589669
RCV000855592
RCV001356295
RCV002225433
RCV004532565
dbSNP Id:
rs146198085
ExAC:
22:29121001 T / G
gnomAD v2:
22-29121001-T-G
gnomAD v3:
22-28725013-T-G
gnomAD v4:
22-28725013-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.28725013T>G , CM000684.2:g.28725013T>G | GRCh38 |
| NC_000022.10:g.29121001T>G , CM000684.1:g.29121001T>G | GRCh37 |
| NC_000022.9:g.27451001T>G | NCBI36 |
| NG_008150.1:g.21822A>C | |
| NG_008150.2:g.21854A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000439346.6:c.556A>C | ENSP00000396903.2:p.Asn186His | |
| ENST00000454252.2:c.*536A>C | ENSP00000387451.2:n.*536A>C | |
| ENST00000711048.1:c.556A>C | ENSP00000518557.1:p.Asn186His | |
| ENST00000402731.6:c.445-90A>C | ENSP00000384835.2:n.445-90A>C | |
| ENST00000404276.6:c.556A>C MANE Select | ENSP00000385747.1:p.Asn186His | |
| ENST00000425190.7:c.-108A>C | ENSP00000390244.2:n.-108A>C | |
| ENST00000649563.1:c.-71-5528A>C | ENSP00000496928.1:n.-71-5528A>C | |
| ENST00000650281.1:c.556A>C | ENSP00000497000.1:p.Asn186His | |
| ENST00000328354.10:c.556A>C | ENSP00000329178.6:p.Asn186His | |
| ENST00000348295.7:c.556A>C | ENSP00000329012.5:p.Asn186His | |
| ENST00000382565.5:c.556A>C | ENSP00000372006.2:p.Asn186His | |
| ENST00000382580.6:c.685A>C | ENSP00000372023.2:p.Asn229His | |
| ENST00000402731.5:c.556A>C | ENSP00000384835.1:p.Asn186His | |
| ENST00000403642.5:c.320-5528A>C | ENSP00000384919.1:n.320-5528A>C | |
| ENST00000404276.5:c.556A>C | ENSP00000385747.1:p.Asn186His | |
| ENST00000405598.5:c.556A>C | ENSP00000386087.1:p.Asn186His | |
| ENST00000416671.5:c.556A>C | ENSP00000402225.1:p.Asn186His | |
| ENST00000417588.5:c.556A>C | ENSP00000412901.1:p.Asn186His | |
| ENST00000425190.6:c.-108A>C | ENSP00000390244.1:n.-108A>C | |
| ENST00000433028.6:c.445-90A>C | ENSP00000403659.1:n.445-90A>C | |
| ENST00000433728.5:c.556A>C | ENSP00000404400.1:p.Asn186His | |
| ENST00000439200.5:c.649A>C | ENSP00000408065.1:p.Asn217His | |
| ENST00000439346.5:c.118A>C | ENSP00000396903.1:p.Asn40His | |
| ENST00000447421.5:c.445-90A>C | ENSP00000397478.2:n.445-90A>C | |
| ENST00000448511.5:c.445-90A>C | ENSP00000404567.1:n.445-90A>C | |
| ENST00000454252.1:c.674A>C | ENSP00000387451.1:n.674A>C | |
| NM_001005735.1:c.685A>C | NP_001005735.1:p.Asn229His | |
| NM_001257387.1:c.-222A>C | NP_001244316.1:n.-222A>C | |
| NM_007194.3:c.556A>C | NP_009125.1:p.Asn186His | |
| NM_145862.2:c.556A>C | NP_665861.1:p.Asn186His | |
| XM_011529839.1:c.715A>C | XP_011528141.1:p.Asn239His | |
| XM_011529840.1:c.715A>C | XP_011528142.1:p.Asn239His | |
| XM_011529841.1:c.574-90A>C | XP_011528143.1:n.574-90A>C | |
| XM_011529842.1:c.475-90A>C | XP_011528144.1:n.475-90A>C | |
| XM_011529843.1:c.445-90A>C | XP_011528145.1:n.445-90A>C | |
| XM_011529844.1:c.715A>C | XP_011528146.1:p.Asn239His | |
| XM_011529845.1:c.-108A>C | XP_011528147.1:n.-108A>C | |
| XR_937805.1:n.777A>C | ||
| XR_937806.1:n.772A>C | ||
| XR_937807.1:n.772A>C | ||
| NM_001349956.1:c.445-90A>C | NP_001336885.1:n.445-90A>C | |
| NM_007194.4:c.556A>C MANE Select | NP_009125.1:p.Asn186His | |
| XM_011529839.2:c.715A>C | XP_011528141.1:p.Asn239His | |
| XM_011529840.3:c.715A>C | XP_011528142.1:p.Asn239His | |
| XM_011529842.2:c.475-90A>C | XP_011528144.1:n.475-90A>C | |
| XM_011529844.2:c.715A>C | XP_011528146.1:p.Asn239His | |
| XM_011529845.2:c.-108A>C | XP_011528147.1:n.-108A>C | |
| XM_017028560.1:c.679A>C | XP_016884049.1:p.Asn227His | |
| XM_024452148.1:c.586A>C | XP_024307916.1:p.Asn196His | |
| XM_024452149.1:c.586A>C | XP_024307917.1:p.Asn196His | |
| XR_937805.2:n.788A>C | ||
| XR_937806.2:n.788A>C | ||
| XR_937807.2:n.788A>C | ||
| NM_001005735.2:c.685A>C | NP_001005735.1:p.Asn229His | |
| NM_001257387.2:c.-222A>C | NP_001244316.1:n.-222A>C | |
| NM_001349956.2:c.445-90A>C | NP_001336885.1:n.445-90A>C |