Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94780467C>T , CM000672.2:g.94780467C>T | GRCh38 |
| NC_000010.10:g.96540224C>T , CM000672.1:g.96540224C>T | GRCh37 |
| NC_000010.9:g.96530214C>T | NCBI36 |
| NG_008384.2:g.22762C>T | |
| NG_008384.3:g.22787C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.482-32C>T MANE Select | ENSP00000360372.3:n.482-32C>T | |
| ENST00000645461.1:n.1535-32C>T | ||
| ENST00000371321.7:c.482-32C>T | ENSP00000360372.3:n.482-32C>T | |
| ENST00000464755.1:c.1245-32C>T | ENSP00000483243.1:n.1245-32C>T | |
| NM_000769.2:c.482-32C>T | NP_000760.1:n.482-32C>T | |
| NM_000769.4:c.482-32C>T MANE Select | NP_000760.1:n.482-32C>T |