Canonical Allele Identifier:
CA1859751113
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.82696232C= , CM000671.2:g.82696232C= | GRCh38 |
| NC_000009.11:g.85311147C= , CM000671.1:g.85311147C= | GRCh37 |
| NC_000009.10:g.84500967C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000637606.1:n.986-83647C= | ||
| XR_001746782.1:n.242-83647C= |