Canonical Allele Identifier:
CA1867567617
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.99817185C= , CM000671.2:g.99817185C= | GRCh38 |
| NC_000009.11:g.102579467C= , CM000671.1:g.102579467C= | GRCh37 |
| NC_000009.10:g.101619288C= | NCBI36 |
| NG_028910.1:g.331C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_109802.1:n.69+2636G= |