Linked Data
MyVariant Identifiers:
chr3:g.52258176A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52224160A>C , CM000665.2:g.52224160A>C | GRCh38 |
| NC_000003.11:g.52258176A>C , CM000665.1:g.52258176A>C | GRCh37 |
| NC_000003.10:g.52233216A>C | NCBI36 |
| NG_033933.1:g.7004T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360658.3:c.156T>G MANE Select | ENSP00000353874.2:p.Ser52= | |
| ENST00000360658.2:c.156T>G | ENSP00000353874.2:p.Ser52= | |
| ENST00000478201.1:c.330T>G | ||
| ENST00000494383.1:c.616T>G | ||
| NM_017442.3:c.156T>G | NP_059138.1:p.Ser52= | |
| NM_017442.4:c.156T>G MANE Select | NP_059138.1:p.Ser52= |