Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.8864893C= , CM000670.2:g.8864893C= | GRCh38 |
| NC_000008.10:g.8722403C= , CM000670.1:g.8722403C= | GRCh37 |
| NC_000008.9:g.8759813C= | NCBI36 |
| NG_009444.1:g.33729G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000276282.7:c.2998+25168G= MANE Select | ENSP00000276282.6:n.2998+25168G= | |
| ENST00000276282.6:c.2998+25168G= | ENSP00000276282.6:n.2998+25168G= | |
| NM_004225.2:c.2998+25168G= | NP_004216.2:n.2998+25168G= | |
| XR_246634.2:n.3534+25168G= | ||
| XM_024447330.1:c.2998+25168G= | XP_024303098.1:n.2998+25168G= | |
| NM_004225.3:c.2998+25168G= MANE Select | NP_004216.2:n.2998+25168G= |