Linked Data
dbSNP Id:
rs779892594
ExAC:
19:55666169 C / T
gnomAD v2:
19-55666169-C-T
gnomAD v4:
19-55154801-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154801C>T , CM000681.2:g.55154801C>T | GRCh38 |
| NC_000019.9:g.55666169C>T , CM000681.1:g.55666169C>T | GRCh37 |
| NC_000019.8:g.60357981C>T | NCBI36 |
| NG_007866.2:g.7932G>A , LRG_432:g.7932G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.312G>A MANE Select | ENSP00000341838.5:p.Val104= | |
| ENST00000665070.1:c.312G>A | ENSP00000499482.1:p.Val104= | |
| ENST00000344887.9:c.312G>A | ENSP00000341838.5:p.Val104= | |
| ENST00000585806.5:n.311G>A | ||
| ENST00000586669.5:n.320G>A | ||
| ENST00000587176.5:n.496G>A | ||
| ENST00000587871.1:c.931G>A | ||
| ENST00000588882.1:c.237G>A | ENSP00000466729.1:p.Val79= | |
| ENST00000590463.1:n.484G>A | ||
| NM_000363.4:c.312G>A , LRG_432t1:c.312G>A | NP_000354.4:p.Val104= | |
| NM_000363.5:c.312G>A MANE Select | NP_000354.4:p.Val104= |