Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5043931T= , CM000674.2:g.5043931T= | GRCh38 |
| NC_000012.11:g.5153097T= , CM000674.1:g.5153097T= | GRCh37 |
| NC_000012.10:g.5023358T= | NCBI36 |
| NG_012198.1:g.5013T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.-217T= MANE Select | ENSP00000252321.3:n.-217T= | |
| NM_002234.3:c.-217T= | NP_002225.2:n.-217T= | |
| NM_002234.4:c.-217T= MANE Select | NP_002225.2:n.-217T= |