Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10673001A>T , CM000682.2:g.10673001A>T | GRCh38 |
| NC_000020.10:g.10653649A>T , CM000682.1:g.10653649A>T | GRCh37 |
| NC_000020.9:g.10601649A>T | NCBI36 |
| NG_007496.1:g.6046T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000214.3:c.87T>A MANE Select | NP_000205.1:p.Cys29Ter |
| ENST00000254958.10:c.87T>A MANE Select | ENSP00000254958.4:p.Cys29Ter |
| NM_000214.2:c.87T>A | NP_000205.1:p.Cys29Ter |
| ENST00000254958.9:c.87T>A | ENSP00000254958.4:p.Cys29Ter |