Canonical Allele Identifier:
CA649096902
Gene:
Linked Data
COSMIC:
COSN8945796
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.144559618A>C , CM000666.2:g.144559618A>C | GRCh38 |
| NC_000004.11:g.145480770A>C , CM000666.1:g.145480770A>C | GRCh37 |
| NC_000004.10:g.145700220A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649263.1:c.328-143640T>G | ENSP00000497507.1:n.328-143640T>G | |
| XR_939272.1:n.178+2366T>G | ||
| XR_939273.1:n.178+2366T>G | ||
| XR_939272.2:n.522+2366T>G | ||
| XR_939273.2:n.522+2366T>G |