Canonical Allele Identifier:
CA647127939
Gene:
Linked Data
COSMIC:
COSN7332343
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122884131C>T , CM000664.2:g.122884131C>T | GRCh38 |
| NC_000002.11:g.123641707C>T , CM000664.1:g.123641707C>T | GRCh37 |
| NC_000002.10:g.123358177C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923292.1:n.1125-811C>T | ||
| XR_001739692.1:n.1451-811C>T | ||
| XR_923292.2:n.1358-811C>T |