Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31583901T>C , CM000664.2:g.31583901T>C | GRCh38 |
| NC_000002.11:g.31808970T>C , CM000664.1:g.31808970T>C | GRCh37 |
| NC_000002.10:g.31662474T>C | NCBI36 |
| NG_008365.1:g.2071A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XM_011533070.1:c.27-50135A>G | XP_011531372.1:n.27-50135A>G |
| XM_011533071.1:c.27-50135A>G | XP_011531373.1:n.27-50135A>G |
| XM_011533072.1:c.27-50135A>G | XP_011531374.1:n.27-50135A>G |
| XM_011533072.2:c.27-50135A>G | XP_011531374.1:n.27-50135A>G |