Canonical Allele Identifier:
CA1216113098
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193121736A= , CM000663.2:g.193121736A= | GRCh38 |
| NC_000001.10:g.193090866A= , CM000663.1:g.193090866A= | GRCh37 |
| NC_000001.9:g.191357489A= | NCBI36 |
| NG_012691.1:g.4779A= , LRG_507:g.4779A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001738350.1:n.1921T= |