Linked Data
ClinVar Variation Id:
382048
dbSNP Id:
rs780024263
ExAC:
16:5129051 T / C
gnomAD v2:
16-5129051-T-C
gnomAD v3:
16-5079050-T-C
gnomAD v4:
16-5079050-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.5079050T>C , CM000678.2:g.5079050T>C | GRCh38 |
| NC_000016.9:g.5129051T>C , CM000678.1:g.5129051T>C | GRCh37 |
| NC_000016.8:g.5069052T>C | NCBI36 |
| NG_009202.1:g.12242T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000592793.6:n.3001-16T>C | ||
| ENST00000682020.1:c.269-14T>C | ENSP00000508075.1:n.269-14T>C | |
| ENST00000682206.1:c.863-14T>C | ENSP00000508285.1:n.863-14T>C | |
| ENST00000682314.1:n.907-14T>C | ||
| ENST00000682327.1:c.373+172T>C | ENSP00000507058.1:n.373+172T>C | |
| ENST00000682349.1:n.3001-14T>C | ||
| ENST00000682703.1:n.3172T>C | ||
| ENST00000682797.1:c.863-14T>C | ENSP00000507582.1:n.863-14T>C | |
| ENST00000682985.1:c.374-14T>C | ENSP00000507598.1:n.374-14T>C | |
| ENST00000683433.1:c.157+172T>C | ENSP00000507463.1:n.157+172T>C | |
| ENST00000683685.1:n.1078T>C | ||
| ENST00000683710.1:c.*826-14T>C | ENSP00000506785.1:n.*826-14T>C | |
| ENST00000683739.1:c.530-14T>C | ENSP00000507002.1:n.530-14T>C | |
| ENST00000683772.1:n.907-14T>C | ||
| ENST00000684008.1:c.797-14T>C | ENSP00000507962.1:n.797-14T>C | |
| ENST00000684190.1:c.862+172T>C | ENSP00000507554.1:n.862+172T>C | |
| ENST00000684335.1:c.863-14T>C | ENSP00000508112.1:n.863-14T>C | |
| ENST00000262374.10:c.863-14T>C MANE Select | ENSP00000262374.5:n.863-14T>C | |
| ENST00000650085.1:n.1683-14T>C | ||
| ENST00000262374.9:c.863-14T>C | ENSP00000262374.4:n.863-14T>C | |
| ENST00000544428.1:c.530-14T>C | ENSP00000440019.1:n.530-14T>C | |
| ENST00000588623.5:c.530-14T>C | ENSP00000468118.1:n.530-14T>C | |
| ENST00000591822.5:c.*764-14T>C | ENSP00000467865.1:n.*764-14T>C | |
| NM_019109.4:c.863-14T>C | NP_061982.3:n.863-14T>C | |
| XM_011522565.1:c.530-14T>C | XP_011520867.1:n.530-14T>C | |
| XR_932882.1:n.904-14T>C | ||
| NM_001330504.1:c.530-14T>C | NP_001317433.1:n.530-14T>C | |
| XM_017023457.2:c.862+172T>C | XP_016878946.1:n.862+172T>C | |
| XM_017023458.1:c.530-14T>C | XP_016878947.1:n.530-14T>C | |
| XR_932882.3:n.888-14T>C | ||
| NM_019109.5:c.863-14T>C MANE Select | NP_061982.3:n.863-14T>C | |
| NM_001330504.2:c.530-14T>C | NP_001317433.1:n.530-14T>C |