Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63072921T>C , CM000670.2:g.63072921T>C | GRCh38 |
| NC_000008.10:g.63985480T>C , CM000670.1:g.63985480T>C | GRCh37 |
| NC_000008.9:g.64148034T>C | NCBI36 |
| NG_016123.1:g.18133A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260116.5:c.358+14A>G MANE Select | ENSP00000260116.4:n.358+14A>G | |
| ENST00000260116.4:c.358+14A>G | ENSP00000260116.4:n.358+14A>G | |
| ENST00000521138.1:n.232+12897A>G | ||
| NM_000370.3:c.358+14A>G MANE Select | NP_000361.1:n.358+14A>G | |
| XM_006716468.2:c.205-8605A>G | XP_006716531.1:n.205-8605A>G | |
| XM_006716468.4:c.205-8605A>G | XP_006716531.1:n.205-8605A>G |