Linked Data
ClinVar Variation Id:
1645361
ClinVar RCV Id:
RCV002148491
dbSNP Id:
rs750956651
ExAC:
3:48605263 C / T
gnomAD v2:
3-48605263-C-T
gnomAD v3:
3-48567830-C-T
gnomAD v4:
3-48567830-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.48567830C>T , CM000665.2:g.48567830C>T | GRCh38 |
| NC_000003.11:g.48605263C>T , CM000665.1:g.48605263C>T | GRCh37 |
| NC_000003.10:g.48580267C>T | NCBI36 |
| NG_007065.1:g.32423G>A , LRG_286:g.32423G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000681320.1:c.7929+8G>A MANE Select | ENSP00000506558.1:n.7929+8G>A | |
| ENST00000328333.12:c.7929+8G>A | ENSP00000332371.8:n.7929+8G>A | |
| ENST00000459756.5:n.752+8G>A | ||
| ENST00000487017.5:n.4568+8G>A | ||
| NM_000094.3:c.7929+8G>A , LRG_286t1:c.7929+8G>A | NP_000085.1:n.7929+8G>A | |
| XM_011533336.1:c.7956+8G>A | XP_011531638.1:n.7956+8G>A | |
| XM_011533337.1:c.7929+8G>A | XP_011531639.1:n.7929+8G>A | |
| XM_011533338.1:c.7896+8G>A | XP_011531640.1:n.7896+8G>A | |
| XR_940369.1:n.7992+8G>A | ||
| XR_940370.1:n.7992+8G>A | ||
| XR_940371.1:n.7992+8G>A | ||
| XM_017005688.1:c.7869+8G>A | XP_016861177.1:n.7869+8G>A | |
| XR_001740003.1:n.7965+8G>A | ||
| XR_001740004.1:n.7965+8G>A | ||
| XR_001740005.1:n.7965+8G>A | ||
| NM_000094.4:c.7929+8G>A MANE Select | NP_000085.1:n.7929+8G>A |