Canonical Allele Identifier:
CA1910164286
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.52573815T>G , CM000672.2:g.52573815T>G | GRCh38 |
| NC_000010.10:g.54333575T>G , CM000672.1:g.54333575T>G | GRCh37 |
| NC_000010.9:g.54003581T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_945961.1:n.379-12700A>C | ||
| XR_945962.1:n.383-12700A>C | ||
| NR_155748.1:n.96-12700A>C | ||
| XR_001747449.2:n.108-12700A>C | ||
| XR_001747450.2:n.329-12700A>C | ||
| XR_945961.3:n.9426-12700A>C | ||
| XR_945962.3:n.9430-12700A>C |