Canonical Allele Identifier:
CA473651083
Gene:
Linked Data
MyVariant Identifiers:
chr11:g.27505621C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.27484074C>T , CM000673.2:g.27484074C>T | GRCh38 |
| NC_000011.9:g.27505621C>T , CM000673.1:g.27505621C>T | GRCh37 |
| NC_000011.8:g.27462197C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496450.1:n.225C>T |