gnomAD v2:
gnomAD v3:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40008196G>T , CM000677.2:g.40008196G>T | GRCh38 |
| NC_000015.9:g.40300397G>T , CM000677.1:g.40300397G>T | GRCh37 |
| NC_000015.8:g.38087689G>T | NCBI36 |
| NG_034053.1:g.79073G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263791.10:c.3576+1G>T MANE Select | ENSP00000263791.5:n.3576+1G>T | |
| ENST00000263791.9:c.3576+1G>T | ENSP00000263791.5:n.3576+1G>T | |
| ENST00000558557.1:n.739+1G>T | ||
| ENST00000558629.5:n.2493+1G>T | ||
| ENST00000560855.5:c.2908+1G>T | ||
| NM_001013703.3:c.3576+1G>T | NP_001013725.2:n.3576+1G>T | |
| XM_005254392.1:c.3576+1G>T | XP_005254449.1:n.3576+1G>T | |
| XM_011521599.1:c.3576+1G>T | XP_011519901.1:n.3576+1G>T | |
| XM_011521600.1:c.3576+1G>T | XP_011519902.1:n.3576+1G>T | |
| XM_005254392.3:c.3576+1G>T | XP_005254449.1:n.3576+1G>T | |
| XM_011521599.2:c.3576+1G>T | XP_011519901.1:n.3576+1G>T | |
| XM_011521600.3:c.3576+1G>T | XP_011519902.1:n.3576+1G>T | |
| XM_017022219.2:c.3576+1G>T | XP_016877708.1:n.3576+1G>T | |
| NM_001013703.4:c.3576+1G>T MANE Select | NP_001013725.2:n.3576+1G>T |