Canonical Allele Identifier:
CA10758089
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.240704176C>T , CM000663.2:g.240704176C>T | GRCh38 |
| NC_000001.10:g.240867476C>T , CM000663.1:g.240867476C>T | GRCh37 |
| NC_000001.9:g.238934099C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_949320.1:n.74+5770G>A | ||
| XR_949320.2:n.124+5770G>A |