Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102798678T>C , CM000673.2:g.102798678T>C | GRCh38 |
| NC_000011.9:g.102669409T>C , CM000673.1:g.102669409T>C | GRCh37 |
| NC_000011.8:g.102174619T>C | NCBI36 |
| NG_011740.1:g.4558A>G | |
| NG_011740.2:g.4558A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_038390.1:n.682+556T>C | |
| ENST00000371455.7:n.423+556T>C | |
| ENST00000525739.6:n.682+556T>C | |
| ENST00000544704.1:n.443+556T>C |