Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.4862548T>G , CM000666.2:g.4862548T>G | GRCh38 |
| NC_000004.11:g.4864275T>G , CM000666.1:g.4864275T>G | GRCh37 |
| NC_000004.10:g.4915176T>G | NCBI36 |
| NG_008121.1:g.7884T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382723.5:c.470-153T>G MANE Select | ENSP00000372170.4:n.470-153T>G | |
| ENST00000382723.4:c.470-153T>G | ENSP00000372170.4:n.470-153T>G | |
| ENST00000468421.1:n.121T>G | ||
| NM_002448.3:c.470-153T>G MANE Select | NP_002439.2:n.470-153T>G |