Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.203857249T= , CM000664.2:g.203857249T= | GRCh38 |
| NC_000002.11:g.204721972T= , CM000664.1:g.204721972T= | GRCh37 |
| NC_000002.10:g.204430217T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696479.1:c.47+3173T= | ENSP00000512655.1:n.47+3173T= | |
| XR_923797.1:n.225-5224T= |