Linked Data
ClinVar Variation Id:
2851771
ClinVar RCV Id:
RCV003691296
MyVariant Identifiers:
chr16:g.731547C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.681547C>T , CM000678.2:g.681547C>T | GRCh38 |
| NC_000016.9:g.731547C>T , CM000678.1:g.731547C>T | GRCh37 |
| NC_000016.8:g.671548C>T | NCBI36 |
| NG_034141.1:g.6437C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000219548.9:c.468C>T (STUB1) MANE Select | ENSP00000219548.4:p.His156= | |
| ENST00000219548.8:c.468C>T (STUB1) | ENSP00000219548.4:p.His156= | |
| ENST00000563505.5:n.564C>T (STUB1) | ||
| ENST00000564316.1:c.67C>T (STUB1) | ||
| ENST00000564370.5:c.252C>T (STUB1) | ENSP00000456875.1:p.His84= | |
| ENST00000565677.5:c.252C>T (STUB1) | ENSP00000457228.1:p.His84= | |
| ENST00000566181.2:n.237C>T (STUB1) | ||
| ENST00000566408.5:c.185C>T (STUB1) | ||
| ENST00000567173.5:c.411C>T (STUB1) | ENSP00000456591.1:p.His137= | |
| ENST00000569248.5:n.1042C>T (STUB1) | ||
| ENST00000620831.4:c.-50+38244C>T (MSLN) | ENSP00000482893.1:n.-50+38244C>T | |
| NM_001293197.1:c.252C>T (STUB1) | NP_001280126.1:p.His84= | |
| NM_005861.3:c.468C>T (STUB1) | NP_005852.2:p.His156= | |
| NM_005861.4:c.468C>T (STUB1) MANE Select | NP_005852.2:p.His156= | |
| NM_001293197.2:c.252C>T (STUB1) | NP_001280126.1:p.His84= |