Canonical Allele Identifier:
CA1835396908
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.15157979T= , CM000671.2:g.15157979T= | GRCh38 |
| NC_000009.11:g.15157977T= , CM000671.1:g.15157977T= | GRCh37 |
| NC_000009.10:g.15147977T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001746624.2:n.879-4928T= | |
| XR_929492.1:n.250-4928T= | |
| XR_929492.3:n.279-4928T= | |
| XR_929493.1:n.194-4928T= | |
| XR_929493.3:n.194-4928T= |