Canonical Allele Identifier:
CA646533535
Gene:
Linked Data
COSMIC:
COSN1804238
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.16458337T>A , CM000664.2:g.16458337T>A | GRCh38 |
| NC_000002.11:g.16639605T>A , CM000664.1:g.16639605T>A | GRCh37 |
| NC_000002.10:g.16503086T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939752.1:n.396-3243A>T |