Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73404198C>A , CM000666.2:g.73404198C>A | GRCh38 |
| NC_000004.11:g.74269915C>A , CM000666.1:g.74269915C>A | GRCh37 |
| NC_000004.10:g.74488779C>A | NCBI36 |
| NG_009291.1:g.4944C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000441319.5:c.48-171C>A | ENSP00000392541.1:n.48-171C>A |