Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10641688C>A , CM000682.2:g.10641688C>A | GRCh38 |
| NC_000020.10:g.10622336C>A , CM000682.1:g.10622336C>A | GRCh37 |
| NC_000020.9:g.10570336C>A | NCBI36 |
| NG_007496.1:g.37359G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.2688G>T MANE Select | ENSP00000254958.4:p.Trp896Cys | |
| ENST00000617965.2:n.3277G>T | ||
| ENST00000254958.9:c.2688G>T | ENSP00000254958.4:p.Trp896Cys | |
| ENST00000423891.6:n.2554G>T | ||
| NM_000214.2:c.2688G>T | NP_000205.1:p.Trp896Cys | |
| NM_000214.3:c.2688G>T MANE Select | NP_000205.1:p.Trp896Cys |