Linked Data
MyVariant Identifiers:
chr12:g.52827630G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52433846G>T , CM000674.2:g.52433846G>T | GRCh38 |
| NC_000012.11:g.52827630G>T , CM000674.1:g.52827630G>T | GRCh37 |
| NC_000012.10:g.51113897G>T | NCBI36 |
| NG_008403.1:g.5481C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252245.6:c.459C>A MANE Select | ENSP00000252245.5:p.Ile153= | |
| ENST00000252245.5:c.459C>A | ENSP00000252245.5:p.Ile153= | |
| NM_004693.2:c.459C>A | NP_004684.2:p.Ile153= | |
| NM_004693.3:c.459C>A MANE Select | NP_004684.2:p.Ile153= |