Linked Data
MyVariant Identifiers:
chr12:g.53045774C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52651990C>T , CM000674.2:g.52651990C>T | GRCh38 |
| NC_000012.11:g.53045774C>T , CM000674.1:g.53045774C>T | GRCh37 |
| NC_000012.10:g.51332041C>T | NCBI36 |
| NG_008296.1:g.5186G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309680.4:c.153G>A MANE Select | ENSP00000310861.3:p.Gly51= | |
| ENST00000309680.3:c.153G>A | ENSP00000310861.3:p.Gly51= | |
| NM_000423.2:c.153G>A | NP_000414.2:p.Gly51= | |
| NM_000423.3:c.153G>A MANE Select | NP_000414.2:p.Gly51= |