Canonical Allele Identifier:
CA1500739522
Gene:
Linked Data
dbSNP Id:
rs1727416914
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.144601613T>G , CM000666.2:g.144601613T>G | GRCh38 |
| NC_000004.11:g.145522765T>G , CM000666.1:g.145522765T>G | GRCh37 |
| NC_000004.10:g.145742215T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000649263.1:c.328-185635A>C | ENSP00000497507.1:n.328-185635A>C |