Canonical Allele Identifier:
CA1841175534
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.25551362T= , CM000671.2:g.25551362T= | GRCh38 |
| NC_000009.11:g.25551360T= , CM000671.1:g.25551360T= | GRCh37 |
| NC_000009.10:g.25541360T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_929525.1:n.50-790A= | ||
| XR_929525.2:n.674-790A= |