Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.72020787T>C , CM000674.2:g.72020787T>C | GRCh38 |
| NC_000012.11:g.72414567T>C , CM000674.1:g.72414567T>C | GRCh37 |
| NC_000012.10:g.70700834T>C | NCBI36 |
| NG_008279.1:g.86942T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000333850.4:c.1069-1612T>C MANE Select | ENSP00000329093.3:n.1069-1612T>C | |
| ENST00000333850.3:c.1069-1612T>C | ENSP00000329093.3:n.1069-1612T>C | |
| NM_173353.3:c.1069-1612T>C | NP_775489.2:n.1069-1612T>C | |
| XM_011537899.1:c.475-1612T>C | XP_011536201.1:n.475-1612T>C | |
| NM_173353.4:c.1069-1612T>C MANE Select | NP_775489.2:n.1069-1612T>C |