Canonical Allele Identifier:
CA1284431867
Gene:
Linked Data
dbSNP Id:
rs1678953459
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122369275T>G , CM000664.2:g.122369275T>G | GRCh38 |
| NC_000002.11:g.123126851T>G , CM000664.1:g.123126851T>G | GRCh37 |
| NC_000002.10:g.122843321T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923278.1:n.556-23688T>G | ||
| XR_001739684.1:n.556-23688T>G |