Linked Data
ClinVar Variation Id:
844689
dbSNP Id:
rs766958196
ExAC:
19:55666159 C / T
gnomAD v2:
19-55666159-C-T
gnomAD v4:
19-55154791-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154791C>T , CM000681.2:g.55154791C>T | GRCh38 |
| NC_000019.9:g.55666159C>T , CM000681.1:g.55666159C>T | GRCh37 |
| NC_000019.8:g.60357971C>T | NCBI36 |
| NG_007866.2:g.7942G>A , LRG_432:g.7942G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.322G>A MANE Select | ENSP00000341838.5:p.Asp108Asn | |
| ENST00000665070.1:c.322G>A | ENSP00000499482.1:p.Asp108Asn | |
| ENST00000344887.9:c.322G>A | ENSP00000341838.5:p.Asp108Asn | |
| ENST00000585806.5:n.321G>A | ||
| ENST00000586669.5:n.330G>A | ||
| ENST00000587176.5:n.506G>A | ||
| ENST00000587871.1:c.941G>A | ||
| ENST00000588882.1:c.247G>A | ENSP00000466729.1:p.Asp83Asn | |
| ENST00000590463.1:n.494G>A | ||
| NM_000363.4:c.322G>A , LRG_432t1:c.322G>A | NP_000354.4:p.Asp108Asn | |
| NM_000363.5:c.322G>A MANE Select | NP_000354.4:p.Asp108Asn |