Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73404236T>C , CM000666.2:g.73404236T>C | GRCh38 |
| NC_000004.11:g.74269953T>C , CM000666.1:g.74269953T>C | GRCh37 |
| NC_000004.10:g.74488817T>C | NCBI36 |
| NG_009291.1:g.4982T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000441319.5:c.48-133T>C | ENSP00000392541.1:n.48-133T>C |