Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.10725229C>A , CM000666.2:g.10725229C>A | GRCh38 |
| NC_000004.11:g.10726853C>A , CM000666.1:g.10726853C>A | GRCh37 |
| NC_000004.10:g.10335951C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XM_011513775.1:c.3+9299G>T | XP_011512077.1:n.3+9299G>T |
| XM_011513775.2:c.3+9299G>T | XP_011512077.1:n.3+9299G>T |
| XM_017007684.1:c.3+9299G>T | XP_016863173.1:n.3+9299G>T |
| XM_017007685.1:c.3+9299G>T | XP_016863174.1:n.3+9299G>T |