Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87863551G>A , CM000672.2:g.87863551G>A | GRCh38 |
| NC_000010.10:g.89623308G>A , CM000672.1:g.89623308G>A | GRCh37 |
| NC_000010.9:g.89613288G>A | NCBI36 |
| NG_007466.2:g.5114G>A , LRG_311:g.5114G>A | |
| NG_033079.1:g.4887C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706954.1:c.-16-903G>A | ENSP00000516674.1:n.-16-903G>A | |
| ENST00000688308.1:c.-17+438G>A | ENSP00000508752.1:n.-17+438G>A | |
| ENST00000693560.1:c.-399G>A | ENSP00000509861.1:n.-399G>A | |
| ENST00000371953.7:c.-919G>A | ENSP00000361021.3:n.-919G>A | |
| ENST00000610634.1:c.-1021G>A | ENSP00000477517.1:n.-1021G>A | |
| NM_000314.5:c.-918G>A | NP_000305.3:n.-918G>A | |
| NM_000314.6:c.-918G>A | NP_000305.3:n.-918G>A | |
| NM_001304717.2:c.-399G>A | NP_001291646.2:n.-399G>A | |
| NM_001304718.1:c.-1623G>A | NP_001291647.1:n.-1623G>A |