Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.106940611T>A , CM000685.2:g.106940611T>A | GRCh38 |
| NC_000023.10:g.106183841T>A , CM000685.1:g.106183841T>A | GRCh37 |
| NC_000023.9:g.106070497T>A | NCBI36 |
| NG_016392.1:g.64634A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000604604.1:c.111+52619A>T | ||
| XM_005262190.3:c.*868A>T | XP_005262247.1:n.*868A>T | |
| XM_006724691.2:c.*868A>T | XP_006724754.1:n.*868A>T | |
| XM_011531027.2:c.*868A>T | XP_011529329.1:n.*868A>T | |
| XM_017029844.1:c.*941A>T | XP_016885333.1:n.*941A>T |