Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.43670289C= , CM000681.2:g.43670289C= | GRCh38 |
| NC_000019.9:g.44174441C= , CM000681.1:g.44174441C= | GRCh37 |
| NC_000019.8:g.48866281C= | NCBI36 |
| NG_032898.1:g.5058G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001005376.2:c.-169G= | NP_001005376.1:n.-169G= |
| NM_001005377.2:c.-169G= | NP_001005377.1:n.-169G= |
| NM_001301037.1:c.-169G= | NP_001287966.1:n.-169G= |
| NM_002659.3:c.-169G= | NP_002650.1:n.-169G= |
| ENST00000221264.8:c.-169G= | ENSP00000221264.3:n.-169G= |
| ENST00000340093.7:c.-169G= | ENSP00000339328.3:n.-169G= |