Linked Data
dbSNP Id:
rs1051715182
gnomAD v2:
1-67724930-C-T
gnomAD v3:
1-67259247-C-T
gnomAD v4:
1-67259247-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.67259247C>T , CM000663.2:g.67259247C>T | GRCh38 |
| NC_000001.10:g.67724930C>T , CM000663.1:g.67724930C>T | GRCh37 |
| NC_000001.9:g.67497518C>T | NCBI36 |
| NG_011498.1:g.97762C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000347310.10:c.*119C>T MANE Select | ENSP00000321345.5:n.*119C>T | |
| ENST00000347310.9:c.*119C>T | ENSP00000321345.5:n.*119C>T | |
| ENST00000395227.2:c.*119C>T | ENSP00000378652.2:n.*119C>T | |
| ENST00000425614.3:c.*119C>T | ENSP00000387640.2:n.*119C>T | |
| ENST00000473881.2:c.*835C>T | ENSP00000486667.1:n.*835C>T | |
| NM_144701.2:c.*119C>T | NP_653302.2:n.*119C>T | |
| XM_005270516.2:c.*119C>T | XP_005270573.1:n.*119C>T | |
| XM_011540789.1:c.*119C>T | XP_011539091.1:n.*119C>T | |
| XM_011540790.1:c.*119C>T | XP_011539092.1:n.*119C>T | |
| XM_011540791.1:c.*119C>T | XP_011539093.1:n.*119C>T | |
| XM_011540790.3:c.*119C>T | XP_011539092.1:n.*119C>T | |
| XM_011540791.3:c.*119C>T | XP_011539093.1:n.*119C>T | |
| NM_144701.3:c.*119C>T MANE Select | NP_653302.2:n.*119C>T |