Linked Data
ClinVar Variation Id:
307569
dbSNP Id:
rs7398298
gnomAD v2:
12-124192728-C-T
gnomAD v3:
12-123708181-C-T
gnomAD v4:
12-123708181-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.123708181C>T , CM000674.2:g.123708181C>T | GRCh38 |
| NC_000012.11:g.124192728C>T , CM000674.1:g.124192728C>T | GRCh37 |
| NC_000012.10:g.122758681C>T | NCBI36 |
| NG_012743.1:g.864C>T | |
| NG_030442.1:g.42069C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303372.7:c.*468C>T MANE Select | ENSP00000304941.5:n.*468C>T | |
| ENST00000679504.1:c.1982-23C>T | ENSP00000505006.1:n.1982-23C>T | |
| ENST00000303372.6:c.*468C>T | ENSP00000304941.5:n.*468C>T | |
| NM_001143850.2:c.*468C>T | NP_001137322.1:n.*468C>T | |
| NM_024809.4:c.*468C>T | NP_079085.2:n.*468C>T | |
| XM_005253623.2:c.*468C>T | XP_005253680.1:n.*468C>T | |
| XM_011538748.1:c.*468C>T | XP_011537050.1:n.*468C>T | |
| XM_017019974.1:c.*468C>T | XP_016875463.1:n.*468C>T | |
| XM_017019975.1:c.*468C>T | XP_016875464.1:n.*468C>T | |
| NM_024809.5:c.*468C>T MANE Select | NP_079085.2:n.*468C>T | |
| NM_001143850.3:c.*468C>T | NP_001137322.1:n.*468C>T |