Canonical Allele Identifier:
CA460228756
Gene:
Linked Data
MyVariant Identifiers:
chr8:g.31034300C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.31176784C>G , CM000670.2:g.31176784C>G | GRCh38 |
| NC_000008.10:g.31034300C>G , CM000670.1:g.31034300C>G | GRCh37 |
| NC_000008.9:g.31153842C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_949642.1:n.313C>G | ||
| XR_949647.1:n.608G>C | ||
| XR_949648.1:n.510G>C |