Linked Data
ClinVar Variation Id:
292336
ClinVar RCV Id:
RCV000273632
dbSNP Id:
rs886045207
gnomAD v4:
1-119759928-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119759928G>A , CM000663.2:g.119759928G>A | GRCh38 |
| NC_000001.10:g.120302551G>A , CM000663.1:g.120302551G>A | GRCh37 |
| NC_000001.9:g.120104074G>A | NCBI36 |
| NG_013348.1:g.14005C>T , LRG_447:g.14005C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369406.8:c.621C>T MANE Select | ENSP00000358414.3:p.Pro207= | |
| ENST00000369406.7:c.621C>T | ENSP00000358414.3:p.Pro207= | |
| ENST00000476640.1:n.517C>T | ||
| ENST00000544913.2:c.560-646C>T | ENSP00000439495.2:n.560-646C>T | |
| NM_001166107.1:c.560-646C>T , LRG_447t2:c.560-646C>T | NP_001159579.1:n.560-646C>T | |
| NM_005518.3:c.621C>T , LRG_447t1:c.621C>T | NP_005509.1:p.Pro207= | |
| XM_011541313.1:c.621C>T | XP_011539615.1:p.Pro207= | |
| XM_011541313.2:c.621C>T | XP_011539615.1:p.Pro207= | |
| NM_005518.4:c.621C>T MANE Select | NP_005509.1:p.Pro207= |