Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52224162A>T , CM000665.2:g.52224162A>T | GRCh38 |
| NC_000003.11:g.52258178A>T , CM000665.1:g.52258178A>T | GRCh37 |
| NC_000003.10:g.52233218A>T | NCBI36 |
| NG_033933.1:g.7002T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360658.3:c.154T>A MANE Select | ENSP00000353874.2:p.Ser52Thr | |
| ENST00000360658.2:c.154T>A | ENSP00000353874.2:p.Ser52Thr | |
| ENST00000478201.1:c.328T>A | ||
| ENST00000494383.1:c.614T>A | ||
| NM_017442.3:c.154T>A | NP_059138.1:p.Ser52Thr | |
| NM_017442.4:c.154T>A MANE Select | NP_059138.1:p.Ser52Thr |