Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.71938866G= , CM000674.2:g.71938866G= | GRCh38 |
| NC_000012.11:g.72332646G= , CM000674.1:g.72332646G= | GRCh37 |
| NC_000012.10:g.70618913G= | NCBI36 |
| NG_008279.1:g.5021G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000333850.4:c.-121G= MANE Select | ENSP00000329093.3:n.-121G= | |
| ENST00000333850.3:c.-121G= | ENSP00000329093.3:n.-121G= | |
| NM_173353.3:c.-121G= | NP_775489.2:n.-121G= | |
| NM_173353.4:c.-121G= MANE Select | NP_775489.2:n.-121G= |