Canonical Allele Identifier:
CA2700304700
Gene:
Linked Data
dbSNP Id:
rs2104681928
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122369390T>C , CM000664.2:g.122369390T>C | GRCh38 |
| NC_000002.11:g.123126966T>C , CM000664.1:g.123126966T>C | GRCh37 |
| NC_000002.10:g.122843436T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923278.1:n.556-23573T>C | ||
| XR_001739684.1:n.556-23573T>C |