Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.13765774T>C , CM000686.2:g.13765774T>C | GRCh38 |
| NC_000024.9:g.15877654T>C , CM000686.1:g.15877654T>C | GRCh37 |
| NC_000024.8:g.14387048T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000430079.5:n.429+10985T>C | |
| ENST00000460561.1:n.212+10985T>C | |
| ENST00000472227.5:n.350+13769T>C | |
| ENST00000652544.1:n.684+10985T>C |