Canonical Allele Identifier:
CA1468682193
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.74554149C= , CM000666.2:g.74554149C= | GRCh38 |
| NC_000004.11:g.75419866C= , CM000666.1:g.75419866C= | GRCh37 |
| NC_000004.10:g.75638730C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741513.1:n.167-1317G= |