Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10658624C= , CM000682.2:g.10658624C= | GRCh38 |
| NC_000020.10:g.10639272C= , CM000682.1:g.10639272C= | GRCh37 |
| NC_000020.9:g.10587272C= | NCBI36 |
| NG_007496.1:g.20423G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.538G= MANE Select | ENSP00000254958.4:p.Glu180= | |
| ENST00000254958.9:c.538G= | ENSP00000254958.4:p.Glu180= | |
| ENST00000423891.6:n.404G= | ||
| NM_000214.2:c.538G= | NP_000205.1:p.Glu180= | |
| NM_000214.3:c.538G= MANE Select | NP_000205.1:p.Glu180= |