Linked Data
MyVariant Identifiers:
chr12:g.52910546G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52516762G>A , CM000674.2:g.52516762G>A | GRCh38 |
| NC_000012.11:g.52910546G>A , CM000674.1:g.52910546G>A | GRCh37 |
| NC_000012.10:g.51196813G>A | NCBI36 |
| NG_008297.1:g.8698C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.1314C>T MANE Select | ENSP00000252242.4:p.Ala438= | |
| ENST00000252242.8:c.1314C>T | ENSP00000252242.4:p.Ala438= | |
| ENST00000547890.5:n.692C>T | ||
| ENST00000548409.5:c.436C>T | ||
| ENST00000549511.5:n.521C>T | ||
| ENST00000552629.5:n.1412C>T | ||
| NM_000424.3:c.1314C>T | NP_000415.2:p.Ala438= | |
| NM_000424.4:c.1314C>T MANE Select | NP_000415.2:p.Ala438= |