Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.203866277T= , CM000664.2:g.203866277T= | GRCh38 |
| NC_000002.11:g.204731000T= , CM000664.1:g.204731000T= | GRCh37 |
| NC_000002.10:g.204439245T= | NCBI36 |
| NG_011502.1:g.3492T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696479.1:c.48-1641T= | ENSP00000512655.1:n.48-1641T= |