Canonical Allele Identifier:
CA1365145722
Gene:
Linked Data
dbSNP Id:
rs1575464947
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.53057229T>G , CM000665.2:g.53057229T>G | GRCh38 |
| NC_000003.11:g.53091245T>G , CM000665.1:g.53091245T>G | GRCh37 |
| NC_000003.10:g.53066285T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000607203.1:c.318-9990A>C | ||
| ENST00000607283.5:c.465-13975A>C | ||
| ENST00000607495.5:c.447+20459A>C |