Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151526728T= , CM000668.2:g.151526728T= | GRCh38 |
| NC_000006.11:g.151847863T= , CM000668.1:g.151847863T= | GRCh37 |
| NC_000006.10:g.151889556T= | NCBI36 |
| NG_021198.1:g.37689T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239374.8:c.58-9590T= MANE Select | ENSP00000239374.6:n.58-9590T= | |
| ENST00000239374.7:c.58-9590T= | ENSP00000239374.6:n.58-9590T= | |
| NM_025059.3:c.58-9590T= | NP_079335.2:n.58-9590T= | |
| NM_025059.4:c.58-9590T= MANE Select | NP_079335.2:n.58-9590T= |