Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.203856977T= , CM000664.2:g.203856977T= | GRCh38 |
| NC_000002.11:g.204721700T= , CM000664.1:g.204721700T= | GRCh37 |
| NC_000002.10:g.204429945T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696479.1:c.47+2901T= | ENSP00000512655.1:n.47+2901T= | |
| XR_923797.1:n.225-5496T= |