Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81215330T= , CM000678.2:g.81215330T= | GRCh38 |
| NC_000016.9:g.81248935T= , CM000678.1:g.81248935T= | GRCh37 |
| NC_000016.8:g.79806436T= | NCBI36 |
| NG_033236.1:g.10041A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337114.8:c.464-136A= | ENSP00000337397.4:n.464-136A= | |
| ENST00000525539.5:c.464-136A= | ENSP00000434417.1:n.464-136A= | |
| ENST00000614230.4:c.464-136A= | ENSP00000483832.1:n.464-136A= | |
| NM_001076780.1:c.464-136A= | NP_001070248.1:n.464-136A= | |
| NM_052892.3:c.464-136A= | NP_443124.3:n.464-136A= | |
| NR_126532.1:n.464-136A= | ||
| NM_001076780.2:c.464-136A= | NP_001070248.1:n.464-136A= | |
| NM_052892.4:c.464-136A= | NP_443124.3:n.464-136A= | |
| NR_126532.2:n.488-136A= |