Canonical Allele Identifier:
CA1500738993
Gene:
Linked Data
dbSNP Id:
rs1578785900
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.144601370G>A , CM000666.2:g.144601370G>A | GRCh38 |
| NC_000004.11:g.145522522G>A , CM000666.1:g.145522522G>A | GRCh37 |
| NC_000004.10:g.145741972G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649263.1:c.328-185392C>T | ENSP00000497507.1:n.328-185392C>T |