Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10141351T>C , CM000665.2:g.10141351T>C | GRCh38 |
| NC_000003.11:g.10183035T>C , CM000665.1:g.10183035T>C | GRCh37 |
| NC_000003.10:g.10158035T>C | NCBI36 |
| NG_008212.3:g.4717T>C , LRG_322:g.4717T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000256474.2:c.-497T>C | ENSP00000256474.2:n.-497T>C |