Linked Data
ClinVar Variation Id:
2885682
ClinVar RCV Id:
RCV003717372
dbSNP Id:
rs1851000075
gnomAD v4:
10-49482674-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.49482674C>T , CM000672.2:g.49482674C>T | GRCh38 |
| NC_000010.10:g.50690720C>T , CM000672.1:g.50690720C>T | GRCh37 |
| NC_000010.9:g.50360726C>T | NCBI36 |
| NG_009442.1:g.61428G>A , LRG_465:g.61428G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355832.10:c.2169+13G>A MANE Select | ENSP00000348089.5:n.2169+13G>A | |
| ENST00000681632.1:n.2247+13G>A | ||
| ENST00000681659.1:c.2010+13G>A | ENSP00000505631.1:n.2010+13G>A | |
| ENST00000355832.9:c.2169+13G>A | ENSP00000348089.5:n.2169+13G>A | |
| ENST00000623073.3:c.*561+13G>A | ENSP00000485650.1:n.*561+13G>A | |
| ENST00000623115.3:c.279+13G>A | ENSP00000485321.1:n.279+13G>A | |
| NM_000124.3:c.2169+13G>A | NP_000115.1:n.2169+13G>A | |
| NM_001346440.1:c.2169+13G>A | NP_001333369.1:n.2169+13G>A | |
| NM_000124.4:c.2169+13G>A MANE Select | NP_000115.1:n.2169+13G>A | |
| NM_001346440.2:c.2169+13G>A | NP_001333369.1:n.2169+13G>A |