Canonical Allele Identifier:
CA278487092
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13919990C>G , CM000678.2:g.13919990C>G | GRCh38 |
| NC_000016.9:g.14013847C>G , CM000678.1:g.14013847C>G | GRCh37 |
| NC_000016.8:g.13921348C>G | NCBI36 |
| NG_011442.1:g.4834C>G , LRG_463:g.4834C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_933098.1:n.82+6535G>C | |
| XR_933099.1:n.82+6535G>C | |
| XR_933100.1:n.82+6535G>C |