Linked Data
dbSNP Id:
rs4149311
gnomAD v2:
9-107588777-C-T
gnomAD v3:
9-104826496-C-T
gnomAD v4:
9-104826496-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.104826496C>T , CM000671.2:g.104826496C>T | GRCh38 |
| NC_000009.11:g.107588777C>T , CM000671.1:g.107588777C>T | GRCh37 |
| NC_000009.10:g.106628598C>T | NCBI36 |
| NG_007981.1:g.106660G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000374736.8:c.2337+452G>A MANE Select | ENSP00000363868.3:n.2337+452G>A | |
| ENST00000678995.1:c.2337+452G>A | ENSP00000504612.1:n.2337+452G>A | |
| ENST00000374736.7:c.2337+452G>A | ENSP00000363868.3:n.2337+452G>A | |
| ENST00000494467.1:n.510+452G>A | ||
| NM_005502.3:c.2337+452G>A | NP_005493.2:n.2337+452G>A | |
| XM_005251773.1:c.2337+452G>A | XP_005251830.1:n.2337+452G>A | |
| XM_005251776.1:c.2157+452G>A | XP_005251833.1:n.2157+452G>A | |
| XM_011518339.1:c.2412+452G>A | XP_011516641.1:n.2412+452G>A | |
| XM_011518340.1:c.2412+452G>A | XP_011516642.1:n.2412+452G>A | |
| XM_011518341.1:c.2412+452G>A | XP_011516643.1:n.2412+452G>A | |
| XM_011518342.1:c.1974+452G>A | XP_011516644.1:n.1974+452G>A | |
| XM_011518343.1:c.2412+452G>A | XP_011516645.1:n.2412+452G>A | |
| XM_011518344.1:c.2412+452G>A | XP_011516646.1:n.2412+452G>A | |
| XM_005251773.3:c.2337+452G>A | XP_005251830.1:n.2337+452G>A | |
| XM_005251776.3:c.2157+452G>A | XP_005251833.1:n.2157+452G>A | |
| XM_011518339.3:c.2412+452G>A | XP_011516641.1:n.2412+452G>A | |
| XM_011518340.3:c.2412+452G>A | XP_011516642.1:n.2412+452G>A | |
| XM_011518341.3:c.2412+452G>A | XP_011516643.1:n.2412+452G>A | |
| XM_011518342.3:c.1974+452G>A | XP_011516644.1:n.1974+452G>A | |
| XM_011518344.2:c.2412+452G>A | XP_011516646.1:n.2412+452G>A | |
| XM_017014378.2:c.2412+452G>A | XP_016869867.1:n.2412+452G>A | |
| XM_017014379.2:c.2412+452G>A | XP_016869868.1:n.2412+452G>A | |
| XM_017014380.2:c.2412+452G>A | XP_016869869.1:n.2412+452G>A | |
| XM_017014381.2:c.2412+452G>A | XP_016869870.1:n.2412+452G>A | |
| XM_017014382.2:c.2274+452G>A | XP_016869871.1:n.2274+452G>A | |
| XR_001746223.1:n.2725+452G>A | ||
| NM_005502.4:c.2337+452G>A MANE Select | NP_005493.2:n.2337+452G>A |