Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.217041133T>C , CM000664.2:g.217041133T>C | GRCh38 |
| NC_000002.11:g.217905856T>C , CM000664.1:g.217905856T>C | GRCh37 |
| NC_000002.10:g.217614101T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_923881.1:n.299+47115T>C | ||
| XR_923883.1:n.294+47115T>C | ||
| XR_923885.1:n.862+47115T>C | ||
| XR_923886.1:n.359-14058T>C | ||
| XR_923887.1:n.300-14058T>C | ||
| XR_001739169.1:n.11844+47115T>C | ||
| XR_001739170.2:n.8480+47115T>C | ||
| XR_001739171.2:n.8347+47115T>C | ||
| XR_923878.2:n.7446T>C |