Linked Data
MyVariant Identifiers:
chr12:g.5021687G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4912521G>T , CM000674.2:g.4912521G>T | GRCh38 |
| NC_000012.11:g.5021687G>T , CM000674.1:g.5021687G>T | GRCh37 |
| NC_000012.10:g.4891948G>T | NCBI36 |
| NG_011815.1:g.7615G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.1143G>T MANE Select | ENSP00000371985.3:p.Val381= | |
| ENST00000543874.3:n.105+2049G>T | ||
| ENST00000639306.1:c.981G>T | ENSP00000492506.1:p.Val327= | |
| ENST00000639680.1:c.76+255G>T | ||
| ENST00000382545.3:c.1143G>T | ENSP00000371985.3:p.Val381= | |
| ENST00000541095.1:n.105+2049G>T | ||
| ENST00000543874.2:n.96+2049G>T | ||
| NM_000217.2:c.1143G>T | NP_000208.2:p.Val381= | |
| NM_000217.3:c.1143G>T MANE Select | NP_000208.2:p.Val381= |