Linked Data
ClinVar Variation Id:
496268
dbSNP Id:
rs755825264
ExAC:
3:14209830 G / A
gnomAD v2:
3-14209830-G-A
gnomAD v3:
3-14168330-G-A
gnomAD v4:
3-14168330-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14168330G>A , CM000665.2:g.14168330G>A | GRCh38 |
| NC_000003.11:g.14209830G>A , CM000665.1:g.14209830G>A | GRCh37 |
| NC_000003.10:g.14184834G>A | NCBI36 |
| NG_011763.1:g.15343C>T , LRG_472:g.15343C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000285021.12:c.463C>T MANE Select | ENSP00000285021.8:p.Arg155Ter | |
| ENST00000285021.11:c.463C>T | ENSP00000285021.7:p.Arg155Ter | |
| ENST00000452172.1:n.228C>T | ||
| ENST00000455144.6:n.74C>T | ||
| ENST00000476581.6:c.413-1077C>T | ENSP00000424548.1:n.413-1077C>T | |
| ENST00000511155.1:c.445C>T | ENSP00000423867.1:p.Arg149Ter | |
| NM_004628.4:c.463C>T , LRG_472t1:c.463C>T | NP_004619.3:p.Arg155Ter | |
| NR_027299.1:n.517-1077C>T | ||
| XM_011534092.1:c.463C>T | XP_011532394.1:p.Arg155Ter | |
| XM_011534093.1:c.463C>T | XP_011532395.1:p.Arg155Ter | |
| NM_001354726.1:c.-43-1077C>T | NP_001341655.1:n.-43-1077C>T | |
| NM_001354727.1:c.463C>T | NP_001341656.1:p.Arg155Ter | |
| NM_001354729.1:c.445C>T | NP_001341658.1:p.Arg149Ter | |
| NM_001354730.1:c.463C>T | NP_001341659.1:p.Arg155Ter | |
| NR_148950.1:n.567C>T | ||
| NR_148951.1:n.517-1077C>T | ||
| XR_001740256.2:n.496C>T | ||
| XR_002959580.1:n.496C>T | ||
| XR_002959581.1:n.496C>T | ||
| NM_001354727.2:c.463C>T | NP_001341656.1:p.Arg155Ter | |
| NM_004628.5:c.463C>T MANE Select | NP_004619.3:p.Arg155Ter | |
| NR_148950.2:n.496C>T | ||
| NR_148951.2:n.446-1077C>T | ||
| NM_001354726.2:c.-43-1077C>T | NP_001341655.1:n.-43-1077C>T | |
| NM_001354729.2:c.445C>T | NP_001341658.1:p.Arg149Ter | |
| NM_001354730.2:c.463C>T | NP_001341659.1:p.Arg155Ter |