Canonical Allele Identifier:
CA650461138
Gene:
Linked Data
COSMIC:
COSN20488877
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.465902G>T , CM000668.2:g.465902G>T | GRCh38 |
| NC_000006.11:g.465902G>T , CM000668.1:g.465902G>T | GRCh37 |
| NC_000006.10:g.410902G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_926364.1:n.2714+12177G>T | ||
| XR_926365.1:n.2548+12177G>T | ||
| XR_001743914.1:n.482-9306G>T |