Canonical Allele Identifier:
CA1149396935
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.2036459C= , CM000663.2:g.2036459C= | GRCh38 |
| NC_000001.10:g.1967898C= , CM000663.1:g.1967898C= | GRCh37 |
| NC_000001.9:g.1957758C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_946823.1:n.749G= | ||
| XR_001737845.2:n.752G= | ||
| XR_946823.3:n.752G= |