Linked Data
ClinVar Variation Id:
187734
dbSNP Id:
rs398122611
ExAC:
13:32954231 T / C
gnomAD v2:
13-32954231-T-C
gnomAD v3:
13-32380094-T-C
gnomAD v4:
13-32380094-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32380094T>C , CM000675.2:g.32380094T>C | GRCh38 |
| NC_000013.10:g.32954231T>C , CM000675.1:g.32954231T>C | GRCh37 |
| NC_000013.9:g.31852231T>C | NCBI36 |
| NG_012772.3:g.69615T>C , LRG_293:g.69615T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.9205T>C | ENSP00000434898.2:p.Cys3069Arg | |
| ENST00000528762.2:c.*572T>C | ENSP00000433168.2:n.*572T>C | |
| ENST00000530893.7:c.8836T>C | ENSP00000499438.2:p.Cys2946Arg | |
| ENST00000665585.2:c.*767T>C | ENSP00000499570.2:n.*767T>C | |
| ENST00000666593.2:c.9205T>C | ENSP00000499256.2:p.Cys3069Arg | |
| ENST00000700202.2:c.9154T>C | ENSP00000514856.2:p.Cys3052Arg | |
| ENST00000700202.1:c.1621T>C | ENSP00000514856.1:p.Cys541Arg | |
| ENST00000700203.1:n.1332T>C | ||
| ENST00000380152.8:c.9205T>C MANE Select | ENSP00000369497.3:p.Cys3069Arg | |
| ENST00000544455.6:c.9205T>C | ENSP00000439902.1:p.Cys3069Arg | |
| ENST00000614259.2:c.9213T>C | ENSP00000506251.1:n.9213T>C | |
| ENST00000665585.1:c.2083T>C | ||
| ENST00000666593.1:c.88T>C | ENSP00000499256.1:p.Cys30Arg | |
| ENST00000680887.1:c.9205T>C | ENSP00000505508.1:p.Cys3069Arg | |
| ENST00000380152.7:c.9205T>C | ENSP00000369497.3:p.Cys3069Arg | |
| ENST00000470094.1:c.162T>C | ||
| ENST00000544455.5:c.9205T>C | ENSP00000439902.1:p.Cys3069Arg | |
| NM_000059.3:c.9205T>C , LRG_293t1:c.9205T>C | NP_000050.2:p.Cys3069Arg | |
| XM_011535203.1:c.9205T>C | XP_011533505.1:p.Cys3069Arg | |
| XM_011535204.1:c.9109T>C | XP_011533506.1:p.Cys3037Arg | |
| NM_000059.4:c.9205T>C MANE Select | NP_000050.3:p.Cys3069Arg |