Canonical Allele Identifier:
CA1775343139
Gene:
Linked Data
dbSNP Id:
rs1802342074
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.33808330C>T , CM000670.2:g.33808330C>T | GRCh38 |
| NC_000008.10:g.33665848C>T , CM000670.1:g.33665848C>T | GRCh37 |
| NC_000008.9:g.33785390C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_949659.1:n.240+11894C>T | ||
| XR_002956701.1:n.240+11894C>T |