Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56639314A>T , CM000678.2:g.56639314A>T | GRCh38 |
| NC_000016.9:g.56673226A>T , CM000678.1:g.56673226A>T | GRCh37 |
| NC_000016.8:g.55230727A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290705.12:c.79A>T MANE Select | ENSP00000290705.8:p.Thr27Ser | |
| ENST00000622334.1:c.79A>T | ENSP00000478425.1:p.Thr27Ser | |
| NM_005946.2:c.79A>T | NP_005937.2:p.Thr27Ser | |
| NM_005946.3:c.79A>T MANE Select | NP_005937.2:p.Thr27Ser |