Linked Data
ClinVar Variation Id:
1634069
ClinVar RCV Id:
RCV002124327
dbSNP Id:
rs1229858789
gnomAD v2:
1-45973232-G-A
gnomAD v4:
1-45507560-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45507560G>A , CM000663.2:g.45507560G>A | GRCh38 |
| NC_000001.10:g.45973232G>A , CM000663.1:g.45973232G>A | GRCh37 |
| NC_000001.9:g.45745819G>A | NCBI36 |
| NG_013378.1:g.12377G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000401061.9:c.276+10G>A MANE Select | ENSP00000383840.4:n.276+10G>A | |
| ENST00000401061.8:c.276+10G>A | ENSP00000383840.4:n.276+10G>A | |
| ENST00000616135.1:c.105+10G>A | ENSP00000478859.1:n.105+10G>A | |
| NM_015506.2:c.276+10G>A | NP_056321.2:n.276+10G>A | |
| XM_005270724.3:c.82-652G>A | XP_005270781.1:n.82-652G>A | |
| XM_011541204.1:c.105+10G>A | XP_011539506.1:n.105+10G>A | |
| NM_001330540.1:c.105+10G>A | NP_001317469.1:n.105+10G>A | |
| XM_005270724.5:c.82-652G>A | XP_005270781.1:n.82-652G>A | |
| NM_015506.3:c.276+10G>A MANE Select | NP_056321.2:n.276+10G>A | |
| NM_001330540.2:c.105+10G>A | NP_001317469.1:n.105+10G>A |