Linked Data
MyVariant Identifiers:
chr12:g.5021120G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4911954G>T , CM000674.2:g.4911954G>T | GRCh38 |
| NC_000012.11:g.5021120G>T , CM000674.1:g.5021120G>T | GRCh37 |
| NC_000012.10:g.4891381G>T | NCBI36 |
| NG_011815.1:g.7048G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000382545.5:c.576G>T MANE Select | ENSP00000371985.3:p.Leu192= | |
| ENST00000543874.3:n.105+1482G>T | ||
| ENST00000639306.1:c.414G>T | ENSP00000492506.1:p.Leu138= | |
| ENST00000382545.3:c.576G>T | ENSP00000371985.3:p.Leu192= | |
| ENST00000541095.1:n.105+1482G>T | ||
| ENST00000543874.2:n.96+1482G>T | ||
| NM_000217.2:c.576G>T | NP_000208.2:p.Leu192= | |
| NM_000217.3:c.576G>T MANE Select | NP_000208.2:p.Leu192= |