Canonical Allele Identifier:
CA1485692005
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.111874141T= , CM000666.2:g.111874141T= | GRCh38 |
| NC_000004.11:g.112795297T= , CM000666.1:g.112795297T= | GRCh37 |
| NC_000004.10:g.113014746T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939076.1:n.170+23835T= | ||
| XR_939077.1:n.659+23835T= | ||
| XR_939076.2:n.170+23835T= | ||
| XR_939077.2:n.668+23835T= |