Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55125462T= , CM000666.2:g.55125462T= | GRCh38 |
| NC_000004.11:g.55991629T= , CM000666.1:g.55991629T= | GRCh37 |
| NC_000004.10:g.55686386T= | NCBI36 |
| NG_012004.1:g.5134A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.-169A= MANE Select | ENSP00000263923.4:n.-169A= | |
| ENST00000263923.4:c.-169A= | ENSP00000263923.4:n.-169A= | |
| NM_002253.2:c.-169A= | NP_002244.1:n.-169A= | |
| NM_002253.3:c.-169A= | NP_002244.1:n.-169A= | |
| NM_002253.4:c.-169A= MANE Select | NP_002244.1:n.-169A= |