Canonical Allele Identifier:
CA1320446123
Gene:
Linked Data
dbSNP Id:
rs2077888745
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.200033121C>A , CM000664.2:g.200033121C>A | GRCh38 |
| NC_000002.11:g.200897844C>A , CM000664.1:g.200897844C>A | GRCh37 |
| NC_000002.10:g.200606089C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923778.1:n.178-22225G>T |