Linked Data
dbSNP Id:
rs150882026
gnomAD v2:
8-1244227-C-T
gnomAD v3:
8-1295967-C-T
gnomAD v4:
8-1295967-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.1295967C>T , CM000670.2:g.1295967C>T | GRCh38 |
| NC_000008.10:g.1244227C>T , CM000670.1:g.1244227C>T | GRCh37 |
| NC_000008.9:g.1231634C>T | NCBI36 |
| NG_009409.2:g.563249C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000421627.7:c.103+37084C>T | ENSP00000400258.3:n.103+37084C>T | |
| ENST00000637795.2:c.106+37084C>T MANE Select | ENSP00000489774.1:n.106+37084C>T | |
| XM_011534761.1:c.-135+37084C>T | XP_011533063.1:n.-135+37084C>T | |
| XM_011534762.1:c.-135+37084C>T | XP_011533064.1:n.-135+37084C>T | |
| NM_001346810.1:c.106+37084C>T | NP_001333739.1:n.106+37084C>T | |
| NM_001346810.2:c.106+37084C>T MANE Select | NP_001333739.1:n.106+37084C>T |