Canonical Allele Identifier:
CA1168497147
Gene:
Linked Data
dbSNP Id:
rs1557430678
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.56262284G>A , CM000663.2:g.56262284G>A | GRCh38 |
| NC_000001.10:g.56727956G>A , CM000663.1:g.56727956G>A | GRCh37 |
| NC_000001.9:g.56500544G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641109.1:c.760-13084C>T | ENSP00000493138.1:n.760-13084C>T | |
| ENST00000641346.1:c.367-13084C>T | ||
| ENST00000641415.1:c.193-8391C>T | ||
| ENST00000641494.1:c.379-13084C>T | ||
| ENST00000642129.1:c.769-13084C>T |