Canonical Allele Identifier:
CA1600919267
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.171724227T= , CM000667.2:g.171724227T= | GRCh38 |
| NC_000005.9:g.171151231T= , CM000667.1:g.171151231T= | GRCh37 |
| NC_000005.8:g.171083836T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001742980.1:n.3391A= | |
| XR_001742981.1:n.3306A= | |
| XR_001742982.1:n.3179A= | |
| XR_001742983.1:n.1628+1677A= | |
| XR_001742984.1:n.3253A= | |
| XR_941218.2:n.2991A= | |
| XR_941219.1:n.3633A= | |
| XR_941220.1:n.1956+1677A= |