Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154379248T= , CM000685.2:g.154379248T= | GRCh38 |
| NC_000023.10:g.153607608T= , CM000685.1:g.153607608T= | GRCh37 |
| NC_000023.9:g.153260802T= | NCBI36 |
| NG_008677.1:g.9813T= , LRG_745:g.9813T= | |
| NG_011506.1:g.399A= | |
| NG_011506.2:g.391A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369842.8:c.-237T= | ENSP00000358857.4:n.-237T= | |
| NM_000117.2:c.-237T= , LRG_745t1:c.-237T= | NP_000108.1:n.-237T= | |
| XM_024452349.1:c.-445T= | XP_024308117.1:n.-445T= |