Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.172902G>A , CM000678.2:g.172902G>A | GRCh38 |
| NC_000016.9:g.222901G>A , CM000678.1:g.222901G>A | GRCh37 |
| NC_000016.8:g.162901G>A | NCBI36 |
| NG_000006.1:g.33765G>A | |
| NG_059186.1:g.1252G>A | |
| NG_059271.1:g.5056G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.-11G>A MANE Select | ENSP00000251595.6:n.-11G>A | |
| ENST00000251595.10:c.-11G>A | ENSP00000251595.6:n.-11G>A | |
| ENST00000397806.1:c.-58G>A | ENSP00000380908.1:n.-58G>A | |
| ENST00000482565.1:n.9G>A | ||
| NM_000517.4:c.-11G>A | NP_000508.1:n.-11G>A | |
| NM_000517.6:c.-11G>A MANE Select | NP_000508.1:n.-11G>A |