Linked Data
ClinVar Variation Id:
409567
dbSNP Id:
rs770449225
ExAC:
13:32953923 A / G
gnomAD v2:
13-32953923-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32379786A>G , CM000675.2:g.32379786A>G | GRCh38 |
| NC_000013.10:g.32953923A>G , CM000675.1:g.32953923A>G | GRCh37 |
| NC_000013.9:g.31851923A>G | NCBI36 |
| NG_012772.3:g.69307A>G , LRG_293:g.69307A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.8990A>G | ENSP00000434898.2:p.Tyr2997Cys | |
| ENST00000528762.2:c.*357A>G | ENSP00000433168.2:n.*357A>G | |
| ENST00000530893.7:c.8621A>G | ENSP00000499438.2:p.Tyr2874Cys | |
| ENST00000665585.2:c.*552A>G | ENSP00000499570.2:n.*552A>G | |
| ENST00000666593.2:c.8990A>G | ENSP00000499256.2:p.Tyr2997Cys | |
| ENST00000700202.2:c.8954-15A>G | ENSP00000514856.2:n.8954-15A>G | |
| ENST00000700202.1:c.1421-15A>G | ENSP00000514856.1:n.1421-15A>G | |
| ENST00000700203.1:n.1117A>G | ||
| ENST00000380152.8:c.8990A>G MANE Select | ENSP00000369497.3:p.Tyr2997Cys | |
| ENST00000544455.6:c.8990A>G | ENSP00000439902.1:p.Tyr2997Cys | |
| ENST00000614259.2:c.8998A>G | ENSP00000506251.1:n.8998A>G | |
| ENST00000665585.1:c.1868A>G | ||
| ENST00000680887.1:c.8990A>G | ENSP00000505508.1:p.Tyr2997Cys | |
| ENST00000380152.7:c.8990A>G | ENSP00000369497.3:p.Tyr2997Cys | |
| ENST00000544455.5:c.8990A>G | ENSP00000439902.1:p.Tyr2997Cys | |
| NM_000059.3:c.8990A>G , LRG_293t1:c.8990A>G | NP_000050.2:p.Tyr2997Cys | |
| XM_011535203.1:c.8990A>G | XP_011533505.1:p.Tyr2997Cys | |
| XM_011535204.1:c.8894A>G | XP_011533506.1:p.Tyr2965Cys | |
| XM_011535205.1:c.*28A>G | XP_011533507.1:n.*28A>G | |
| NM_000059.4:c.8990A>G MANE Select | NP_000050.3:p.Tyr2997Cys |