Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17047413C>A , CM000672.2:g.17047413C>A | GRCh38 |
| NC_000010.10:g.17089412C>A , CM000672.1:g.17089412C>A | GRCh37 |
| NC_000010.9:g.17129418C>A | NCBI36 |
| NG_008967.1:g.87405G>T , LRG_540:g.87405G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001081.4:c.3329+1G>T MANE Select | NP_001072.2:n.3329+1G>T |
| ENST00000377833.10:c.3329+1G>T MANE Select | ENSP00000367064.4:n.3329+1G>T |
| NM_001081.3:c.3329+1G>T , LRG_540t1:c.3329+1G>T | NP_001072.2:n.3329+1G>T |
| ENST00000377833.8:c.3329+1G>T | ENSP00000367064.4:n.3329+1G>T |
| XM_011519708.1:c.3329+1G>T | XP_011518010.1:n.3329+1G>T |
| XM_011519708.2:c.3329+1G>T | XP_011518010.1:n.3329+1G>T |