Canonical Allele Identifier:
CA2737384070
Gene:
Linked Data
dbSNP Id:
rs2123449064
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.22259298C>T , CM000683.2:g.22259298C>T | GRCh38 |
| NC_000021.8:g.23631618C>T , CM000683.1:g.23631618C>T | GRCh37 |
| NC_000021.7:g.22553489C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001754978.1:n.221+46485C>T |