Linked Data
ClinVar Variation Id:
2758111
ClinVar RCV Id:
RCV003569532
MyVariant Identifiers:
chr15:g.85383794T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.84840563T>C , CM000677.2:g.84840563T>C | GRCh38 |
| NC_000015.9:g.85383794T>C , CM000677.1:g.85383794T>C | GRCh37 |
| NC_000015.8:g.83184798T>C | NCBI36 |
| NG_054748.1:g.28933T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258888.6:c.1284T>C MANE Select | ENSP00000258888.6:p.Pro428= | |
| ENST00000258888.5:c.1890T>C | ENSP00000258888.5:p.Pro630= | |
| NM_020778.4:c.1890T>C | NP_065829.3:p.Pro630= | |
| NM_020778.5:c.1284T>C MANE Select | NP_065829.4:p.Pro428= |