Canonical Allele Identifier:
CA2206404162
Gene:
Linked Data
dbSNP Id:
rs539398087
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.9249470G>T , CM000678.2:g.9249470G>T | GRCh38 |
| NC_000016.9:g.9343327G>T , CM000678.1:g.9343327G>T | GRCh37 |
| NC_000016.8:g.9250828G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_933054.1:n.70+64737G>T |