Canonical Allele Identifier:
CA1320446161
Gene:
Linked Data
dbSNP Id:
rs2077889057
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.200033204A>T , CM000664.2:g.200033204A>T | GRCh38 |
| NC_000002.11:g.200897927A>T , CM000664.1:g.200897927A>T | GRCh37 |
| NC_000002.10:g.200606172A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923778.1:n.178-22308T>A |