Linked Data
MyVariant Identifiers:
chr12:g.52845362G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52451578G>T , CM000674.2:g.52451578G>T | GRCh38 |
| NC_000012.11:g.52845362G>T , CM000674.1:g.52845362G>T | GRCh37 |
| NC_000012.10:g.51131629G>T | NCBI36 |
| NG_008299.1:g.5549C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252252.4:c.501C>A MANE Select | ENSP00000252252.3:p.Ile167= | |
| ENST00000252252.3:c.501C>A | ENSP00000252252.3:p.Ile167= | |
| NM_005555.3:c.501C>A | NP_005546.2:p.Ile167= | |
| NM_005555.4:c.501C>A MANE Select | NP_005546.2:p.Ile167= |