Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.37217401T>C , CM000684.2:g.37217401T>C | GRCh38 |
| NC_000022.10:g.37613441T>C , CM000684.1:g.37613441T>C | GRCh37 |
| NC_000022.9:g.35943387T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_005261721.3:c.-37+3006A>G | XP_005261778.1:n.-37+3006A>G | |
| XM_011530349.1:c.-694-1513A>G | XP_011528651.1:n.-694-1513A>G | |
| XM_005261721.4:c.-37+3006A>G | XP_005261778.1:n.-37+3006A>G | |
| XM_011530349.2:c.-694-1513A>G | XP_011528651.1:n.-694-1513A>G | |
| XM_017028924.1:c.-437-1513A>G | XP_016884413.1:n.-437-1513A>G |