Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.216998673T= , CM000664.2:g.216998673T= | GRCh38 |
| NC_000002.11:g.217863396T= , CM000664.1:g.217863396T= | GRCh37 |
| NC_000002.10:g.217571641T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923881.1:n.299+4655T= | ||
| XR_923883.1:n.294+4655T= | ||
| XR_923885.1:n.862+4655T= | ||
| XR_923886.1:n.300-2374T= | ||
| XR_923887.1:n.299+4655T= | ||
| XR_001739169.1:n.11844+4655T= | ||
| XR_001739170.2:n.8480+4655T= | ||
| XR_001739171.2:n.8347+4655T= |