Canonical Allele Identifier:
CA648645975
Gene:
Linked Data
COSMIC:
COSN21766241
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12578256T>G , CM000666.2:g.12578256T>G | GRCh38 |
| NC_000004.11:g.12579880T>G , CM000666.1:g.12579880T>G | GRCh37 |
| NC_000004.10:g.12188978T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_925406.1:n.106+31086A>C | ||
| XR_001741374.1:n.254+44399A>C | ||
| XR_925406.3:n.140+31086A>C |