Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.39920010C>G , CM000670.2:g.39920010C>G | GRCh38 |
| NC_000008.10:g.39777529C>G , CM000670.1:g.39777529C>G | GRCh37 |
| NC_000008.9:g.39896686C>G | NCBI36 |
| NG_028155.1:g.11202C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000518237.6:c.423-90C>G MANE Select | ENSP00000430950.1:n.423-90C>G | |
| ENST00000253513.11:c.433+1066C>G | ENSP00000253513.7:n.433+1066C>G | |
| ENST00000518237.5:c.423-90C>G | ENSP00000430950.1:n.423-90C>G | |
| ENST00000519154.5:c.423-90C>G | ENSP00000428716.1:n.423-90C>G | |
| ENST00000521636.1:n.326-90C>G | ||
| ENST00000522495.5:c.423-90C>G | ENSP00000430505.1:n.423-90C>G | |
| NM_002164.5:c.423-90C>G | NP_002155.1:n.423-90C>G | |
| NM_002164.6:c.423-90C>G MANE Select | NP_002155.1:n.423-90C>G |