Canonical Allele Identifier:
CA2493232079
Gene:
Linked Data
dbSNP Id:
rs1691635658
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.20485675C>T , CM000664.2:g.20485675C>T | GRCh38 |
| NC_000002.11:g.20685436C>T , CM000664.1:g.20685436C>T | GRCh37 |
| NC_000002.10:g.20548917C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_157978.1:n.530+3063G>A |