Canonical Allele Identifier:
CA1439213007
Gene:
Linked Data
dbSNP Id:
rs974722968
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12578388G>T , CM000666.2:g.12578388G>T | GRCh38 |
| NC_000004.11:g.12580012G>T , CM000666.1:g.12580012G>T | GRCh37 |
| NC_000004.10:g.12189110G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_925406.1:n.106+30954C>A | ||
| XR_001741374.1:n.254+44267C>A | ||
| XR_925406.3:n.140+30954C>A |