Linked Data
ClinVar Variation Id:
410235
ClinVar RCV Id:
RCV000471056
dbSNP Id:
rs747274078
ExAC:
10:121429471 C / T
gnomAD v2:
10-121429471-C-T
gnomAD v4:
10-119669959-C-T
COSMIC:
COSM427143
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119669959C>T , CM000672.2:g.119669959C>T | GRCh38 |
| NC_000010.10:g.121429471C>T , CM000672.1:g.121429471C>T | GRCh37 |
| NC_000010.9:g.121419461C>T | NCBI36 |
| NG_016125.1:g.23590C>T , LRG_742:g.23590C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.289C>T MANE Select | ENSP00000358081.4:p.Pro97Ser | |
| ENST00000369085.7:c.289C>T | ENSP00000358081.3:p.Pro97Ser | |
| ENST00000450186.1:c.115C>T | ENSP00000410036.1:p.Pro39Ser | |
| NM_004281.3:c.289C>T , LRG_742t1:c.289C>T | NP_004272.2:p.Pro97Ser | |
| XM_005270287.1:c.289C>T | XP_005270344.1:p.Pro97Ser | |
| XM_005270287.2:c.289C>T | XP_005270344.1:p.Pro97Ser | |
| NM_004281.4:c.289C>T MANE Select | NP_004272.2:p.Pro97Ser |