Canonical Allele Identifier:
CA1205765938
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.168649219G= , CM000663.2:g.168649219G= | GRCh38 |
| NC_000001.10:g.168618457G= , CM000663.1:g.168618457G= | GRCh37 |
| NC_000001.9:g.166885081G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922259.1:n.201-7944C= | ||
| XR_922259.2:n.332-7944C= |