Linked Data
ClinVar Variation Id:
194152
dbSNP Id:
rs114896216
ExAC:
10:50682268 G / A
gnomAD v2:
10-50682268-G-A
gnomAD v3:
10-49474222-G-A
gnomAD v4:
10-49474222-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.49474222G>A , CM000672.2:g.49474222G>A | GRCh38 |
| NC_000010.10:g.50682268G>A , CM000672.1:g.50682268G>A | GRCh37 |
| NC_000010.9:g.50352274G>A | NCBI36 |
| NG_009442.1:g.69880C>T , LRG_465:g.69880C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000355832.10:c.2403C>T MANE Select | ENSP00000348089.5:p.Ala801= | |
| ENST00000681632.1:n.2481C>T | ||
| ENST00000681659.1:c.2244C>T | ENSP00000505631.1:p.Ala748= | |
| ENST00000355832.9:c.2403C>T | ENSP00000348089.5:p.Ala801= | |
| ENST00000623073.3:c.*699C>T | ENSP00000485650.1:n.*699C>T | |
| ENST00000623115.3:c.513C>T | ENSP00000485321.1:p.Ala171= | |
| ENST00000624341.3:c.235C>T | ||
| NM_000124.3:c.2403C>T | NP_000115.1:p.Ala801= | |
| NM_001346440.1:c.2403C>T | NP_001333369.1:p.Ala801= | |
| NM_000124.4:c.2403C>T MANE Select | NP_000115.1:p.Ala801= | |
| NM_001346440.2:c.2403C>T | NP_001333369.1:p.Ala801= |