Linked Data
ClinVar Variation Id:
1647598
ClinVar RCV Id:
RCV002139181
dbSNP Id:
rs757848836
gnomAD v4:
21-44288336-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44288336C>T , CM000683.2:g.44288336C>T | GRCh38 |
| NC_000021.8:g.45708219C>T , CM000683.1:g.45708219C>T | GRCh37 |
| NC_000021.7:g.44532647C>T | NCBI36 |
| NG_009556.1:g.7457C>T , LRG_18:g.7457C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.539-9C>T MANE Select | ENSP00000291582.5:n.539-9C>T | |
| ENST00000291582.5:c.539-9C>T | ENSP00000291582.5:n.539-9C>T | |
| ENST00000527919.5:n.1083-9C>T | ||
| ENST00000530812.5:n.1091-9C>T | ||
| NM_000383.3:c.539-9C>T | NP_000374.1:n.539-9C>T | |
| XM_011529551.1:c.539-9C>T | XP_011527853.1:n.539-9C>T | |
| NM_000383.4:c.539-9C>T MANE Select | NP_000374.1:n.539-9C>T |