Linked Data
ClinVar Variation Id:
290046
ClinVar RCV Id:
RCV000454208
RCV000497486
RCV000801486
RCV001331377
RCV002522012
RCV003463776
RCV002467720
RCV001833396
RCV004537606
dbSNP Id:
rs201218801
ExAC:
12:88453674 C / T
gnomAD v2:
12-88453674-C-T
gnomAD v3:
12-88059897-C-T
gnomAD v4:
12-88059897-C-T
COSMIC:
COSM4575769
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.88059897C>T , CM000674.2:g.88059897C>T | GRCh38 |
| NC_000012.11:g.88453674C>T , CM000674.1:g.88453674C>T | GRCh37 |
| NC_000012.10:g.86977805C>T | NCBI36 |
| NG_008417.1:g.87320G>A | |
| NG_008417.2:g.87320G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309041.12:c.6654+1G>A | ENSP00000308021.8:n.6654+1G>A | |
| ENST00000547691.8:c.3929+1G>A | ||
| ENST00000552810.6:c.6645+1G>A MANE Select | ENSP00000448012.1:n.6645+1G>A | |
| ENST00000671777.2:n.424+1G>A | ||
| ENST00000672414.2:c.*4651+1G>A | ENSP00000500729.1:n.*4651+1G>A | |
| ENST00000672647.1:n.5005+1G>A | ||
| ENST00000673058.2:c.6523-877G>A | ENSP00000500665.2:n.6523-877G>A | |
| ENST00000674889.1:n.3598+1G>A | ||
| ENST00000674971.1:c.6645+1G>A | ENSP00000502194.1:n.6645+1G>A | |
| ENST00000675230.1:c.6624+1G>A | ENSP00000502503.1:n.6624+1G>A | |
| ENST00000675408.1:c.6480+1G>A | ENSP00000502298.1:n.6480+1G>A | |
| ENST00000675476.1:c.7506+1G>A | ENSP00000502161.1:n.7506+1G>A | |
| ENST00000675628.1:n.6872+1G>A | ||
| ENST00000675794.1:c.*4816+1G>A | ENSP00000502841.1:n.*4816+1G>A | |
| ENST00000675833.1:c.7413+1G>A | ENSP00000502559.1:n.7413+1G>A | |
| ENST00000675894.1:n.2950+1G>A | ||
| ENST00000676074.1:c.6480+1G>A | ENSP00000502079.1:n.6480+1G>A | |
| ENST00000676181.1:n.5573+1G>A | ||
| ENST00000676190.1:n.1084+1G>A | ||
| ENST00000676363.1:n.12371+1G>A | ||
| ENST00000309041.11:c.6651+1G>A | ENSP00000308021.7:n.6651+1G>A | |
| ENST00000547691.6:c.3825+1G>A | ENSP00000446905.1:n.3825+1G>A | |
| ENST00000552810.5:c.6645+1G>A | ENSP00000448012.1:n.6645+1G>A | |
| NM_025114.3:c.6645+1G>A | NP_079390.3:n.6645+1G>A | |
| XM_011538756.1:c.7515+1G>A | XP_011537058.1:n.7515+1G>A | |
| XM_011538757.1:c.7515+1G>A | XP_011537059.1:n.7515+1G>A | |
| XM_011538758.1:c.7512+1G>A | XP_011537060.1:n.7512+1G>A | |
| XM_011538759.1:c.7506+1G>A | XP_011537061.1:n.7506+1G>A | |
| XM_011538760.1:c.7393-877G>A | XP_011537062.1:n.7393-877G>A | |
| XM_011538761.1:c.7350+1G>A | XP_011537063.1:n.7350+1G>A | |
| XM_011538762.1:c.6747+1G>A | XP_011537064.1:n.6747+1G>A | |
| XM_011538763.1:c.6654+1G>A | XP_011537065.1:n.6654+1G>A | |
| XM_011538766.1:c.5976+1G>A | XP_011537068.1:n.5976+1G>A | |
| XR_945163.1:n.967+2877C>T | ||
| XM_011538756.3:c.7515+1G>A | XP_011537058.1:n.7515+1G>A | |
| XM_011538757.3:c.7515+1G>A | XP_011537059.1:n.7515+1G>A | |
| XM_011538758.3:c.7512+1G>A | XP_011537060.1:n.7512+1G>A | |
| XM_011538759.2:c.7506+1G>A | XP_011537061.1:n.7506+1G>A | |
| XM_011538760.2:c.7393-877G>A | XP_011537062.1:n.7393-877G>A | |
| XM_011538761.2:c.7350+1G>A | XP_011537063.1:n.7350+1G>A | |
| XM_011538762.3:c.6747+1G>A | XP_011537064.1:n.6747+1G>A | |
| XM_011538763.3:c.6654+1G>A | XP_011537065.1:n.6654+1G>A | |
| XM_011538766.3:c.5976+1G>A | XP_011537068.1:n.5976+1G>A | |
| XM_017019980.2:c.7384-877G>A | XP_016875469.1:n.7384-877G>A | |
| XM_017019981.2:c.7341+1G>A | XP_016875470.1:n.7341+1G>A | |
| XM_017019982.1:c.7515+1G>A | XP_016875471.1:n.7515+1G>A | |
| XM_017019983.2:c.6633+1G>A | XP_016875472.1:n.6633+1G>A | |
| XR_001748869.1:n.7850+1G>A | ||
| XR_001748870.2:n.7685+1G>A | ||
| NM_025114.4:c.6645+1G>A MANE Select | NP_079390.3:n.6645+1G>A |