Linked Data
ClinVar Variation Id:
1208183
ClinVar RCV Id:
RCV001576411
dbSNP Id:
rs999662
gnomAD v2:
16-56899508-T-G
gnomAD v3:
16-56865596-T-G
gnomAD v4:
16-56865596-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56865596T>G , CM000678.2:g.56865596T>G | GRCh38 |
| NC_000016.9:g.56899508T>G , CM000678.1:g.56899508T>G | GRCh37 |
| NC_000016.8:g.55457009T>G | NCBI36 |
| NG_009386.1:g.5390T>G | |
| NG_009386.2:g.5390T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000563236.6:c.282+79T>G MANE Select | ENSP00000456149.2:n.282+79T>G | |
| ENST00000262502.5:c.282+79T>G | ENSP00000262502.5:n.282+79T>G | |
| ENST00000438926.6:c.282+79T>G | ENSP00000402152.2:n.282+79T>G | |
| ENST00000563236.5:c.282+79T>G | ENSP00000456149.1:n.282+79T>G | |
| ENST00000566786.5:c.282+79T>G | ENSP00000457552.1:n.282+79T>G | |
| NM_000339.2:c.282+79T>G | NP_000330.2:n.282+79T>G | |
| NM_001126107.1:c.282+79T>G | NP_001119579.1:n.282+79T>G | |
| NM_001126108.1:c.282+79T>G | NP_001119580.1:n.282+79T>G | |
| XM_005256119.1:c.282+79T>G | XP_005256176.1:n.282+79T>G | |
| XM_005256119.2:c.282+79T>G | XP_005256176.1:n.282+79T>G | |
| NM_000339.3:c.282+79T>G | NP_000330.3:n.282+79T>G | |
| NM_001126107.2:c.282+79T>G | NP_001119579.2:n.282+79T>G | |
| NM_001126108.2:c.282+79T>G MANE Select | NP_001119580.2:n.282+79T>G |