Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.38851869G>T , CM000675.2:g.38851869G>T | GRCh38 |
| NC_000013.10:g.39426006G>T , CM000675.1:g.39426006G>T | GRCh37 |
| NC_000013.9:g.38324006G>T | NCBI36 |
| NG_008125.2:g.169834G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_207361.6:c.6925+1G>T MANE Select | NP_997244.4:n.6925+1G>T |
| ENST00000280481.9:c.6925+1G>T MANE Select | ENSP00000280481.7:n.6925+1G>T |
| NM_207361.5:c.6925+1G>T | NP_997244.4:n.6925+1G>T |
| ENST00000280481.8:c.6925+1G>T | ENSP00000280481.7:n.6925+1G>T |
| XM_011535057.1:c.6925+1G>T | XP_011533359.1:n.6925+1G>T |