Linked Data
MyVariant Identifiers:
chr12:g.53045786A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52652002A>G , CM000674.2:g.52652002A>G | GRCh38 |
| NC_000012.11:g.53045786A>G , CM000674.1:g.53045786A>G | GRCh37 |
| NC_000012.10:g.51332053A>G | NCBI36 |
| NG_008296.1:g.5174T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309680.4:c.141T>C MANE Select | ENSP00000310861.3:p.Gly47= | |
| ENST00000309680.3:c.141T>C | ENSP00000310861.3:p.Gly47= | |
| NM_000423.2:c.141T>C | NP_000414.2:p.Gly47= | |
| NM_000423.3:c.141T>C MANE Select | NP_000414.2:p.Gly47= |