Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42126022C= , CM000684.2:g.42126022C= | GRCh38 |
| NC_000022.10:g.42522027C= , CM000684.1:g.42522027C= | GRCh37 |
| NC_000022.9:g.40851971C= | NCBI36 |
| NG_008376.4:g.9789G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XM_011529966.1:c.1453-69G= | XP_011528268.1:n.1453-69G= |
| XM_011529967.1:c.1453-69G= | XP_011528269.1:n.1453-69G= |
| XM_011529968.1:c.1453-95G= | XP_011528270.1:n.1453-95G= |
| XM_011529969.1:c.1309-69G= | XP_011528271.1:n.1309-69G= |
| XM_011529970.1:c.1300-69G= | XP_011528272.1:n.1300-69G= |