Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.2856465T>G , CM000686.2:g.2856465T>G | GRCh38 |
| NC_000024.9:g.2724506T>G , CM000686.1:g.2724506T>G | GRCh37 |
| NC_000024.8:g.2784506T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000250784.13:c.532+1694T>G MANE Select | ENSP00000250784.7:n.532+1694T>G | |
| ENST00000250784.12:c.532+1694T>G | ENSP00000250784.7:n.532+1694T>G | |
| ENST00000430575.1:c.559+1694T>G | ENSP00000415317.1:n.559+1694T>G | |
| ENST00000477725.1:n.676+1694T>G | ||
| ENST00000515575.1:n.42+1694T>G | ||
| NM_001008.3:c.532+1694T>G | NP_000999.1:n.532+1694T>G | |
| NM_001008.4:c.532+1694T>G MANE Select | NP_000999.1:n.532+1694T>G |