Linked Data
ClinVar Variation Id:
41450
dbSNP Id:
rs1980869
ExAC:
10:112764594 T / C
gnomAD v2:
10-112764594-T-C
gnomAD v3:
10-111004836-T-C
gnomAD v4:
10-111004836-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.111004836T>C , CM000672.2:g.111004836T>C | GRCh38 |
| NC_000010.10:g.112764594T>C , CM000672.1:g.112764594T>C | GRCh37 |
| NC_000010.9:g.112754584T>C | NCBI36 |
| NG_028922.1:g.90294T>C , LRG_753:g.90294T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265277.10:c.1023+42T>C | ENSP00000265277.5:n.1023+42T>C | |
| ENST00000451838.2:c.78+42T>C | ENSP00000408275.2:n.78+42T>C | |
| ENST00000685059.1:c.1161+42T>C | ENSP00000510210.1:n.1161+42T>C | |
| ENST00000685613.1:c.*157+42T>C | ENSP00000510564.1:n.*157+42T>C | |
| ENST00000687592.1:n.1460+42T>C | ||
| ENST00000688928.1:c.1161+42T>C | ENSP00000509273.1:n.1161+42T>C | |
| ENST00000689118.1:c.1161+42T>C | ENSP00000510554.1:n.1161+42T>C | |
| ENST00000689300.1:c.1161+42T>C | ENSP00000510639.1:n.1161+42T>C | |
| ENST00000689997.1:c.78+42T>C | ENSP00000510700.1:n.78+42T>C | |
| ENST00000691369.1:c.1161+42T>C | ENSP00000509754.1:n.1161+42T>C | |
| ENST00000691441.1:c.1161+42T>C | ENSP00000509686.1:n.1161+42T>C | |
| ENST00000691903.1:c.1161+42T>C | ENSP00000510314.1:n.1161+42T>C | |
| ENST00000692776.1:c.1161+42T>C | ENSP00000508524.1:n.1161+42T>C | |
| ENST00000369452.9:c.1161+42T>C MANE Select | ENSP00000358464.5:n.1161+42T>C | |
| ENST00000265277.9:c.1023+42T>C | ENSP00000265277.5:n.1023+42T>C | |
| ENST00000369452.8:c.1161+42T>C | ENSP00000358464.4:n.1161+42T>C | |
| ENST00000451838.1:c.531+42T>C | ENSP00000408275.1:n.531+42T>C | |
| ENST00000489390.1:n.375+42T>C | ||
| NM_001269039.1:c.1023+42T>C | NP_001255968.1:n.1023+42T>C | |
| NM_007373.3:c.1161+42T>C , LRG_753t1:c.1161+42T>C | NP_031399.2:n.1161+42T>C | |
| XM_011540216.1:c.78+42T>C | XP_011538518.1:n.78+42T>C | |
| NM_001269039.2:c.1023+42T>C | NP_001255968.1:n.1023+42T>C | |
| NM_001324336.1:c.1161+42T>C | NP_001311265.1:n.1161+42T>C | |
| NM_001324337.1:c.1161+42T>C | NP_001311266.1:n.1161+42T>C | |
| NR_136749.1:n.573+42T>C | ||
| NM_007373.4:c.1161+42T>C MANE Select | NP_031399.2:n.1161+42T>C | |
| NM_001269039.3:c.1023+42T>C | NP_001255968.1:n.1023+42T>C | |
| NM_001324336.2:c.1161+42T>C | NP_001311265.1:n.1161+42T>C | |
| NM_001324337.2:c.1161+42T>C | NP_001311266.1:n.1161+42T>C | |
| NR_136749.2:n.512+42T>C |