Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52224161G= , CM000665.2:g.52224161G= | GRCh38 |
| NC_000003.11:g.52258177G= , CM000665.1:g.52258177G= | GRCh37 |
| NC_000003.10:g.52233217G= | NCBI36 |
| NG_033933.1:g.7003C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360658.3:c.155C= MANE Select | ENSP00000353874.2:p.Ser52= | |
| ENST00000360658.2:c.155C= | ENSP00000353874.2:p.Ser52= | |
| ENST00000478201.1:c.329C= | ||
| ENST00000494383.1:c.615C= | ||
| NM_017442.3:c.155C= | NP_059138.1:p.Ser52= | |
| NM_017442.4:c.155C= MANE Select | NP_059138.1:p.Ser52= |