Linked Data
ClinVar Variation Id:
12206
ClinVar RCV Id:
RCV000012990
dbSNP Id:
rs387906511
COSMIC:
COSM3423574
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3084620C>T , CM000682.2:g.3084620C>T | GRCh38 |
| NC_000020.10:g.3065266C>T , CM000682.1:g.3065266C>T | GRCh37 |
| NC_000020.9:g.3013266C>T | NCBI36 |
| NG_008663.1:g.5105G>A , LRG_715:g.5105G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000380293.3:c.55G>A MANE Select | ENSP00000369647.3:p.Ala19Thr | |
| NM_000490.4:c.55G>A , LRG_715t1:c.55G>A | NP_000481.2:p.Ala19Thr | |
| XM_011529267.1:c.55G>A | XP_011527569.1:p.Ala19Thr | |
| XM_011529267.2:c.55G>A | XP_011527569.1:p.Ala19Thr | |
| NM_000490.5:c.55G>A MANE Select | NP_000481.2:p.Ala19Thr |