Linked Data
dbSNP Id:
rs771687755
ExAC:
12:7945627 C / T
gnomAD v2:
12-7945627-C-T
COSMIC:
COSM4909739
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.7793031C>T , CM000674.2:g.7793031C>T | GRCh38 |
| NC_000012.11:g.7945627C>T , CM000674.1:g.7945627C>T | GRCh37 |
| NC_000012.10:g.7836894C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229307.9:c.233C>T MANE Select | ENSP00000229307.4:p.Thr78Ile | |
| ENST00000229307.8:c.233C>T | ENSP00000229307.4:p.Thr78Ile | |
| ENST00000526286.1:c.233C>T | ENSP00000435288.1:p.Thr78Ile | |
| ENST00000526434.2:n.377C>T | ||
| ENST00000541267.5:c.161C>T | ENSP00000444434.1:p.Thr54Ile | |
| NM_001297698.1:c.233C>T | NP_001284627.1:p.Thr78Ile | |
| NM_024865.3:c.233C>T | NP_079141.2:p.Thr78Ile | |
| XM_011520850.1:c.233C>T | XP_011519152.1:p.Thr78Ile | |
| XM_011520851.1:c.161C>T | XP_011519153.1:p.Thr54Ile | |
| XM_011520852.1:c.-140C>T | XP_011519154.1:n.-140C>T | |
| NM_024865.4:c.233C>T MANE Select | NP_079141.2:p.Thr78Ile | |
| NM_001297698.2:c.233C>T | NP_001284627.1:p.Thr78Ile |