Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.20778590C= , CM000686.2:g.20778590C= | GRCh38 |
| NC_000024.9:g.22940476C= , CM000686.1:g.22940476C= | GRCh37 |
| NC_000024.8:g.21349864C= | NCBI36 |
| NG_032924.1:g.27523C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000629237.2:c.533-919C= MANE Select | ENSP00000486252.1:n.533-919C= | |
| ENST00000629237.1:c.533-919C= | ENSP00000486252.1:n.533-919C= | |
| NM_001039567.2:c.533-919C= | NP_001034656.1:n.533-919C= | |
| XM_011531423.1:c.482-919C= | XP_011529725.1:n.482-919C= | |
| NM_001039567.3:c.533-919C= MANE Select | NP_001034656.1:n.533-919C= |