Linked Data
ClinVar Variation Id:
321764
dbSNP Id:
rs746744341
ExAC:
17:10549103 C / T
gnomAD v2:
17-10549103-C-T
gnomAD v3:
17-10645786-C-T
gnomAD v4:
17-10645786-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10645786C>T , CM000679.2:g.10645786C>T | GRCh38 |
| NC_000017.10:g.10549103C>T , CM000679.1:g.10549103C>T | GRCh37 |
| NC_000017.9:g.10489828C>T | NCBI36 |
| NG_011537.1:g.16513G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000583535.6:c.1062G>A MANE Select | ENSP00000464317.1:p.Thr354= | |
| ENST00000583535.5:c.1062G>A | ENSP00000464317.1:p.Thr354= | |
| NM_002470.3:c.1062G>A | NP_002461.2:p.Thr354= | |
| XM_011523870.1:c.1062G>A | XP_011522172.1:p.Thr354= | |
| XM_011523871.1:c.1062G>A | XP_011522173.1:p.Thr354= | |
| XM_011523872.1:c.1062G>A | XP_011522174.1:p.Thr354= | |
| XM_011523870.3:c.1062G>A | XP_011522172.1:p.Thr354= | |
| XM_011523871.2:c.1062G>A | XP_011522173.1:p.Thr354= | |
| NM_002470.4:c.1062G>A MANE Select | NP_002461.2:p.Thr354= |