Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3225880A= , CM000668.2:g.3225880A= | GRCh38 |
| NC_000006.11:g.3226114A= , CM000668.1:g.3226114A= | GRCh37 |
| NC_000006.10:g.3171113A= | NCBI36 |
| NG_016715.1:g.6855T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259818.8:c.278-69T= MANE Select | ENSP00000259818.6:n.278-69T= | |
| ENST00000680070.1:n.1208-69T= | ||
| ENST00000681707.1:n.1105-69T= | ||
| ENST00000681757.1:n.583-69T= | ||
| ENST00000259818.7:c.278-69T= | ENSP00000259818.6:n.278-69T= | |
| ENST00000473006.1:n.395-69T= | ||
| NM_178012.4:c.278-69T= | NP_821080.1:n.278-69T= | |
| XM_011514571.1:c.62-69T= | XP_011512873.1:n.62-69T= | |
| NM_178012.5:c.278-69T= MANE Select | NP_821080.1:n.278-69T= |