Linked Data
ClinVar Variation Id:
209607
dbSNP Id:
rs206120
gnomAD v2:
13-32891706-A-G
gnomAD v3:
13-32317569-A-G
gnomAD v4:
13-32317569-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32317569A>G , CM000675.2:g.32317569A>G | GRCh38 |
| NC_000013.10:g.32891706A>G , CM000675.1:g.32891706A>G | GRCh37 |
| NC_000013.9:g.31789706A>G | NCBI36 |
| NG_012772.3:g.7090A>G , LRG_293:g.7090A>G | |
| NG_017006.2:g.2795T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.67+1042A>G | ENSP00000434898.2:n.67+1042A>G | |
| ENST00000528762.2:c.67+1042A>G | ENSP00000433168.2:n.67+1042A>G | |
| ENST00000530893.7:c.-303+1046A>G | ENSP00000499438.2:n.-303+1046A>G | |
| ENST00000665585.2:c.67+1042A>G | ENSP00000499570.2:n.67+1042A>G | |
| ENST00000666593.2:c.67+1042A>G | ENSP00000499256.2:n.67+1042A>G | |
| ENST00000700202.2:c.67+1042A>G | ENSP00000514856.2:n.67+1042A>G | |
| ENST00000700200.1:n.191+1042A>G | ||
| ENST00000700201.1:c.67+1042A>G | ENSP00000514855.1:n.67+1042A>G | |
| ENST00000380152.8:c.67+1042A>G MANE Select | ENSP00000369497.3:n.67+1042A>G | |
| ENST00000544455.6:c.67+1042A>G | ENSP00000439902.1:n.67+1042A>G | |
| ENST00000614259.2:c.67+1042A>G | ENSP00000506251.1:n.67+1042A>G | |
| ENST00000680887.1:c.67+1042A>G | ENSP00000505508.1:n.67+1042A>G | |
| ENST00000380152.7:c.67+1042A>G | ENSP00000369497.3:n.67+1042A>G | |
| ENST00000530893.6:n.265+1046A>G | ||
| ENST00000544455.5:c.67+1042A>G | ENSP00000439902.1:n.67+1042A>G | |
| ENST00000614259.1:n.67+1042A>G | ||
| NM_000059.3:c.67+1042A>G , LRG_293t1:c.67+1042A>G | NP_000050.2:n.67+1042A>G | |
| XM_011535203.1:c.67+1042A>G | XP_011533505.1:n.67+1042A>G | |
| XM_011535204.1:c.67+1042A>G | XP_011533506.1:n.67+1042A>G | |
| XM_011535205.1:c.67+1042A>G | XP_011533507.1:n.67+1042A>G | |
| NM_000059.4:c.67+1042A>G MANE Select | NP_000050.3:n.67+1042A>G |