Canonical Allele Identifier:
CA1500737793
Gene:
Linked Data
dbSNP Id:
rs1733826879
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.144559510T>C , CM000666.2:g.144559510T>C | GRCh38 |
| NC_000004.11:g.145480662T>C , CM000666.1:g.145480662T>C | GRCh37 |
| NC_000004.10:g.145700112T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649263.1:c.328-143532A>G | ENSP00000497507.1:n.328-143532A>G | |
| XR_939272.1:n.178+2474A>G | ||
| XR_939273.1:n.178+2474A>G | ||
| XR_939272.2:n.522+2474A>G | ||
| XR_939273.2:n.522+2474A>G |