Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.203866174T= , CM000664.2:g.203866174T= | GRCh38 |
| NC_000002.11:g.204730897T= , CM000664.1:g.204730897T= | GRCh37 |
| NC_000002.10:g.204439142T= | NCBI36 |
| NG_011502.1:g.3389T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696479.1:c.48-1744T= | ENSP00000512655.1:n.48-1744T= |