Linked Data
ClinVar Variation Id:
295900
dbSNP Id:
rs529027225
ExAC:
1:22213834 G / A
gnomAD v2:
1-22213834-G-A
gnomAD v3:
1-21887341-G-A
gnomAD v4:
1-21887341-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.21887341G>A , CM000663.2:g.21887341G>A | GRCh38 |
| NC_000001.10:g.22213834G>A , CM000663.1:g.22213834G>A | GRCh37 |
| NC_000001.9:g.22086421G>A | NCBI36 |
| NG_016740.1:g.54917C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374673.4:c.766-7C>T | ||
| ENST00000374695.8:c.959-7C>T MANE Select | ENSP00000363827.3:n.959-7C>T | |
| ENST00000374673.3:n.439-7C>T | ||
| ENST00000374695.7:c.959-7C>T | ENSP00000363827.3:n.959-7C>T | |
| ENST00000412328.5:n.727-7C>T | ||
| NM_001291860.1:c.959-7C>T | NP_001278789.1:n.959-7C>T | |
| NM_005529.6:c.959-7C>T | NP_005520.4:n.959-7C>T | |
| XM_006710594.2:c.1010-7C>T | XP_006710657.1:n.1010-7C>T | |
| XM_006710595.2:c.959-7C>T | XP_006710658.1:n.959-7C>T | |
| XM_006710596.2:c.1010-7C>T | XP_006710659.1:n.1010-7C>T | |
| XM_006710597.2:c.959-7C>T | XP_006710660.1:n.959-7C>T | |
| XM_011541317.1:c.1010-7C>T | XP_011539619.1:n.1010-7C>T | |
| XM_011541318.1:c.1010-7C>T | XP_011539620.1:n.1010-7C>T | |
| XM_011541319.1:c.1010-7C>T | XP_011539621.1:n.1010-7C>T | |
| XM_011541320.1:c.1010-7C>T | XP_011539622.1:n.1010-7C>T | |
| XM_011541321.1:c.1010-7C>T | XP_011539623.1:n.1010-7C>T | |
| XM_011541322.1:c.1010-7C>T | XP_011539624.1:n.1010-7C>T | |
| XM_011541318.2:c.1010-7C>T | XP_011539620.1:n.1010-7C>T | |
| XM_017001120.1:c.1151-7C>T | XP_016856609.1:n.1151-7C>T | |
| XM_017001121.1:c.1100-7C>T | XP_016856610.1:n.1100-7C>T | |
| XM_017001122.1:c.1100-7C>T | XP_016856611.1:n.1100-7C>T | |
| NM_005529.7:c.959-7C>T MANE Select | NP_005520.4:n.959-7C>T | |
| NM_001291860.2:c.959-7C>T | NP_001278789.1:n.959-7C>T |