Canonical Allele Identifier:
CA1365145597
Gene:
Linked Data
dbSNP Id:
rs1700427402
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.53056968C>T , CM000665.2:g.53056968C>T | GRCh38 |
| NC_000003.11:g.53090984C>T , CM000665.1:g.53090984C>T | GRCh37 |
| NC_000003.10:g.53066024C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000607203.1:c.318-9729G>A | ||
| ENST00000607283.5:c.465-13714G>A | ||
| ENST00000607495.5:c.447+20720G>A |