Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94780778A>G , CM000672.2:g.94780778A>G | GRCh38 |
| NC_000010.10:g.96540535A>G , CM000672.1:g.96540535A>G | GRCh37 |
| NC_000010.9:g.96530525A>G | NCBI36 |
| NG_008384.2:g.23073A>G | |
| NG_008384.3:g.23098A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.642+119A>G MANE Select | ENSP00000360372.3:n.642+119A>G | |
| ENST00000645461.1:n.1695+119A>G | ||
| ENST00000371321.7:c.642+119A>G | ENSP00000360372.3:n.642+119A>G | |
| ENST00000464755.1:c.1405+119A>G | ENSP00000483243.1:n.1405+119A>G | |
| NM_000769.2:c.642+119A>G | NP_000760.1:n.642+119A>G | |
| NM_000769.4:c.642+119A>G MANE Select | NP_000760.1:n.642+119A>G |