Linked Data
gnomAD v4:
5-142143361-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.142143361C>A , CM000667.2:g.142143361C>A | GRCh38 |
| NC_000005.9:g.141522926C>A , CM000667.1:g.141522926C>A | GRCh37 |
| NC_000005.8:g.141503110C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253814.6:c.563-1210C>A MANE Select | ENSP00000253814.3:n.563-1210C>A | |
| ENST00000253814.5:c.563-1210C>A | ENSP00000253814.3:n.563-1210C>A | |
| ENST00000503388.1:n.384C>A | ||
| NM_030571.3:c.563-1210C>A | NP_085048.1:n.563-1210C>A | |
| NM_030571.4:c.563-1210C>A MANE Select | NP_085048.1:n.563-1210C>A |