Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133526980T>C , CM000672.2:g.133526980T>C | GRCh38 |
| NC_000010.10:g.135340484T>C , CM000672.1:g.135340484T>C | GRCh37 |
| NC_000010.9:g.135190474T>C | NCBI36 |
| NG_008383.1:g.4618T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463117.6:c.-40+107T>C | ENSP00000440689.1:n.-40+107T>C | |
| ENST00000541261.1:c.-40+107T>C | ENSP00000437799.1:n.-40+107T>C |