Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32474705G= , CM000684.2:g.32474705G= | GRCh38 |
| NC_000022.10:g.32870692G= , CM000684.1:g.32870692G= | GRCh37 |
| NC_000022.9:g.31200692G= | NCBI36 |
| NG_016001.1:g.4986G= | |
| NG_016001.2:g.4986G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266087.11:c.-298G= | ENSP00000266087.7:n.-298G= | |
| ENST00000420700.5:c.-298G= | ENSP00000406155.1:n.-298G= | |
| XM_011530106.1:c.-471G= | XP_011528408.1:n.-471G= | |
| XM_024452207.1:c.-488G= | XP_024307975.1:n.-488G= |