Canonical Allele Identifier:
CA1905919955
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.43318506C= , CM000672.2:g.43318506C= | GRCh38 |
| NC_000010.10:g.43813954C= , CM000672.1:g.43813954C= | GRCh37 |
| NC_000010.9:g.43133960C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_945902.1:n.19C= | ||
| XR_945902.2:n.109C= |