Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.172912C= , CM000678.2:g.172912C= | GRCh38 |
| NC_000016.9:g.222911C= , CM000678.1:g.222911C= | GRCh37 |
| NC_000016.8:g.162911C= | NCBI36 |
| NG_000006.1:g.33775C= | |
| NG_059186.1:g.1262C= | |
| NG_059271.1:g.5066C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.-1C= MANE Select | ENSP00000251595.6:n.-1C= | |
| ENST00000251595.10:c.-1C= | ENSP00000251595.6:n.-1C= | |
| ENST00000397806.1:c.-48C= | ENSP00000380908.1:n.-48C= | |
| ENST00000482565.1:n.19C= | ||
| NM_000517.4:c.-1C= | NP_000508.1:n.-1C= | |
| NM_000517.6:c.-1C= MANE Select | NP_000508.1:n.-1C= |