Linked Data
ClinVar Variation Id:
1454759
dbSNP Id:
rs2137673220
MyVariant Identifiers:
chr12:g.5021039C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4911873C>T , CM000674.2:g.4911873C>T | GRCh38 |
| NC_000012.11:g.5021039C>T , CM000674.1:g.5021039C>T | GRCh37 |
| NC_000012.10:g.4891300C>T | NCBI36 |
| NG_011815.1:g.6967C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.495C>T MANE Select | ENSP00000371985.3:p.Pro165= | |
| ENST00000543874.3:n.105+1401C>T | ||
| ENST00000639306.1:c.333C>T | ENSP00000492506.1:p.Pro111= | |
| ENST00000382545.3:c.495C>T | ENSP00000371985.3:p.Pro165= | |
| ENST00000541095.1:n.105+1401C>T | ||
| ENST00000543874.2:n.96+1401C>T | ||
| NM_000217.2:c.495C>T | NP_000208.2:p.Pro165= | |
| NM_000217.3:c.495C>T MANE Select | NP_000208.2:p.Pro165= |