Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.111231795T= , CM000664.2:g.111231795T= | GRCh38 |
| NC_000002.11:g.111989372T= , CM000664.1:g.111989372T= | GRCh37 |
| NC_000002.10:g.111705843T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_015395.2:n.2776+1833A= | |
| NR_136161.1:n.749+1833A= | |
| NR_136162.1:n.2581+1833A= | |
| NR_136163.1:n.944+1833A= | |
| NR_136164.1:n.544-23134A= | |
| NR_136165.1:n.548+16353A= | |
| NR_136166.1:n.2581+1833A= | |
| XM_011512259.1:c.-3+1834A= | XP_011510561.1:n.-3+1834A= |
| XM_011512260.1:c.-3+1834A= | XP_011510562.1:n.-3+1834A= |
| XM_011512261.1:c.-1-6581A= | XP_011510563.1:n.-1-6581A= |