Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.114181373A= , CM000665.2:g.114181373A= | GRCh38 |
| NC_000003.11:g.113900220A= , CM000665.1:g.113900220A= | GRCh37 |
| NC_000003.10:g.115382910A= | NCBI36 |
| NG_008842.2:g.23035T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000460779.5:c.-155-2597T= | ENSP00000419402.1:n.-155-2597T= | |
| NM_001282563.2:c.-155-2597T= | NP_001269492.1:n.-155-2597T= | |
| XM_011512510.1:c.-155-2597T= | XP_011510812.1:n.-155-2597T= | |
| XM_011512511.1:c.-155-2597T= | XP_011510813.1:n.-155-2597T= | |
| XM_011512512.1:c.-155-2597T= | XP_011510814.1:n.-155-2597T= | |
| XM_017005829.1:c.-155-2597T= | XP_016861318.1:n.-155-2597T= |