Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48981644G= , CM000674.2:g.48981644G= | GRCh38 |
| NC_000012.11:g.49375427G= , CM000674.1:g.49375427G= | GRCh37 |
| NC_000012.10:g.47661694G= | NCBI36 |
| NG_033141.1:g.8192G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293549.4:c.*4G= MANE Select | ENSP00000293549.3:n.*4G= | |
| ENST00000293549.3:c.*4G= | ENSP00000293549.3:n.*4G= | |
| NM_005430.3:c.*4G= | NP_005421.1:n.*4G= | |
| NM_005430.4:c.*4G= MANE Select | NP_005421.1:n.*4G= |