Linked Data
ClinVar Variation Id:
1143134
ClinVar RCV Id:
RCV001481169
dbSNP Id:
rs2149320953
gnomAD v4:
1-45500423-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45500423T>G , CM000663.2:g.45500423T>G | GRCh38 |
| NC_000001.10:g.45966095T>G , CM000663.1:g.45966095T>G | GRCh37 |
| NC_000001.9:g.45738682T>G | NCBI36 |
| NG_013378.1:g.5240T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000401061.9:c.81+10T>G MANE Select | ENSP00000383840.4:n.81+10T>G | |
| ENST00000401061.8:c.81+10T>G | ENSP00000383840.4:n.81+10T>G | |
| ENST00000616135.1:c.-91+10T>G | ENSP00000478859.1:n.-91+10T>G | |
| NM_015506.2:c.81+10T>G | NP_056321.2:n.81+10T>G | |
| XM_005270724.3:c.81+10T>G | XP_005270781.1:n.81+10T>G | |
| XM_011541204.1:c.-142+10T>G | XP_011539506.1:n.-142+10T>G | |
| NM_001330540.1:c.-142+10T>G | NP_001317469.1:n.-142+10T>G | |
| XM_005270724.5:c.81+10T>G | XP_005270781.1:n.81+10T>G | |
| NM_015506.3:c.81+10T>G MANE Select | NP_056321.2:n.81+10T>G | |
| NM_001330540.2:c.-142+10T>G | NP_001317469.1:n.-142+10T>G |