Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.148994542T>A , CM000667.2:g.148994542T>A | GRCh38 |
| NC_000005.9:g.148374105T>A , CM000667.1:g.148374105T>A | GRCh37 |
| NC_000005.8:g.148354298T>A | NCBI36 |
| NG_007947.2:g.73633A>T , LRG_269:g.73633A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000515425.6:c.*10169A>T MANE Select | ENSP00000423660.1:n.*10169A>T | |
| ENST00000504690.5:c.*12+9184A>T | ENSP00000425627.1:n.*12+9184A>T | |
| ENST00000510350.1:n.231+12339A>T | ||
| NM_024577.3:c.*10169A>T , LRG_269t1:c.*10169A>T | NP_078853.2:n.*10169A>T | |
| NM_024577.4:c.*10169A>T MANE Select | NP_078853.2:n.*10169A>T |