Linked Data
MyVariant Identifiers:
chr12:g.52451585del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52451585del , CM000674.2:g.52451585del | GRCh38 |
| NC_000012.11:g.52845369del , CM000674.1:g.52845369del | GRCh37 |
| NC_000012.10:g.51131636del | NCBI36 |
| NG_008299.1:g.5542del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252252.4:c.494del MANE Select | ENSP00000252252.3:p.Glu165GlyfsTer20 | |
| ENST00000252252.3:c.494del | ENSP00000252252.3:p.Glu165GlyfsTer20 | |
| NM_005555.3:c.494del | NP_005546.2:p.Glu165GlyfsTer20 | |
| NM_005555.4:c.494del MANE Select | NP_005546.2:p.Glu165GlyfsTer20 |