Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586867T= , CM000679.2:g.41586867T= | GRCh38 |
| NC_000017.10:g.39743119T= , CM000679.1:g.39743119T= | GRCh37 |
| NC_000017.9:g.36996645T= | NCBI36 |
| NG_008624.1:g.5029A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.-33A= MANE Select | ENSP00000167586.6:n.-33A= | |
| ENST00000167586.6:c.-33A= | ENSP00000167586.6:n.-33A= | |
| NM_000526.4:c.-33A= | NP_000517.2:n.-33A= | |
| NM_000526.5:c.-33A= MANE Select | NP_000517.3:n.-33A= |