Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.13765676T>C , CM000686.2:g.13765676T>C | GRCh38 |
| NC_000024.9:g.15877556T>C , CM000686.1:g.15877556T>C | GRCh37 |
| NC_000024.8:g.14386950T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000652544.1:n.684+10887T>C | ||
| ENST00000430079.5:n.429+10887T>C | ||
| ENST00000460561.1:n.212+10887T>C | ||
| ENST00000472227.5:n.350+13671T>C |