Linked Data
dbSNP Id:
rs1453221129
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55989533G>C , CM000681.2:g.55989533G>C | GRCh38 |
| NC_000019.9:g.56500899G>C , CM000681.1:g.56500899G>C | GRCh37 |
| NC_000019.8:g.61192711G>C | NCBI36 |
| NG_046924.1:g.7751G>C | |
| NG_051553.1:g.46702G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011526444.1:c.-72+2712G>C | XP_011524746.1:n.-72+2712G>C |