Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.38697788G>A , CM000675.2:g.38697788G>A | GRCh38 |
| NC_000013.10:g.39271925G>A , CM000675.1:g.39271925G>A | GRCh37 |
| NC_000013.9:g.38169925G>A | NCBI36 |
| NG_008125.2:g.15753G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_207361.6:c.5263+1G>A MANE Select | NP_997244.4:n.5263+1G>A |
| ENST00000280481.9:c.5263+1G>A MANE Select | ENSP00000280481.7:n.5263+1G>A |
| NM_207361.5:c.5263+1G>A | NP_997244.4:n.5263+1G>A |
| ENST00000280481.8:c.5263+1G>A | ENSP00000280481.7:n.5263+1G>A |
| XM_011535057.1:c.5263+1G>A | XP_011533359.1:n.5263+1G>A |
| XM_017020554.1:c.5263+1G>A | XP_016876043.1:n.5263+1G>A |
| XR_941571.1:n.5571+1G>A | |
| XR_941571.2:n.5567+1G>A |