Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5046035G= , CM000674.2:g.5046035G= | GRCh38 |
| NC_000012.11:g.5155201G= , CM000674.1:g.5155201G= | GRCh37 |
| NC_000012.10:g.5025462G= | NCBI36 |
| NG_012198.1:g.7117G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.*46G= MANE Select | ENSP00000252321.3:n.*46G= | |
| ENST00000252321.4:c.*46G= | ENSP00000252321.3:n.*46G= | |
| NM_002234.3:c.*46G= | NP_002225.2:n.*46G= | |
| NM_002234.4:c.*46G= MANE Select | NP_002225.2:n.*46G= |