Canonical Allele Identifier:
CA1905919977
Gene:
Linked Data
dbSNP Id:
rs1837178874
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.43318555C>T , CM000672.2:g.43318555C>T | GRCh38 |
| NC_000010.10:g.43814003C>T , CM000672.1:g.43814003C>T | GRCh37 |
| NC_000010.9:g.43134009C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_945902.1:n.68C>T | ||
| XR_945902.2:n.158C>T |