Canonical Allele Identifier:
CA2055289545
Gene:
Linked Data
dbSNP Id:
rs1873068943
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.93293272C>A , CM000674.2:g.93293272C>A | GRCh38 |
| NC_000012.11:g.93687048C>A , CM000674.1:g.93687048C>A | GRCh37 |
| NC_000012.10:g.92211179C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_040096.1:n.329+34755G>T |