Linked Data
dbSNP Id:
rs551704463
ExAC:
4:17493984 G / C
gnomAD v2:
4-17493984-G-C
gnomAD v3:
4-17492361-G-C
gnomAD v4:
4-17492361-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.17492361G>C , CM000666.2:g.17492361G>C | GRCh38 |
| NC_000004.11:g.17493984G>C , CM000666.1:g.17493984G>C | GRCh37 |
| NC_000004.10:g.17103082G>C | NCBI36 |
| NG_008763.1:g.24874C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706645.1:n.1484-21C>G | ||
| ENST00000281243.10:c.437-21C>G MANE Select | ENSP00000281243.5:n.437-21C>G | |
| ENST00000281243.9:c.437-21C>G | ENSP00000281243.5:n.437-21C>G | |
| ENST00000428702.6:c.344-21C>G | ENSP00000390944.2:n.344-21C>G | |
| ENST00000501943.6:n.153C>G | ||
| ENST00000505710.1:c.364-1616C>G | ||
| ENST00000507439.5:c.437-1616C>G | ENSP00000423227.1:n.437-1616C>G | |
| ENST00000508623.5:c.437-5125C>G | ENSP00000426377.1:n.437-5125C>G | |
| ENST00000511609.1:n.148C>G | ||
| ENST00000513615.5:c.437-1616C>G | ENSP00000422759.1:n.437-1616C>G | |
| ENST00000514300.1:c.*368-1616C>G | ENSP00000426039.1:n.*368-1616C>G | |
| NM_000320.2:c.437-21C>G | NP_000311.2:n.437-21C>G | |
| NM_001306140.1:c.344-21C>G | NP_001293069.1:n.344-21C>G | |
| XR_241677.1:n.600-1616C>G | ||
| NR_156494.1:n.617-1616C>G | ||
| NM_000320.3:c.437-21C>G MANE Select | NP_000311.2:n.437-21C>G | |
| NM_001306140.2:c.344-21C>G | NP_001293069.1:n.344-21C>G | |
| NR_156494.2:n.473-1616C>G |