Canonical Allele Identifier:
CA1439212785
Gene:
Linked Data
dbSNP Id:
rs1711582861
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12578144C>T , CM000666.2:g.12578144C>T | GRCh38 |
| NC_000004.11:g.12579768C>T , CM000666.1:g.12579768C>T | GRCh37 |
| NC_000004.10:g.12188866C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_925406.1:n.106+31198G>A | ||
| XR_001741374.1:n.254+44511G>A | ||
| XR_925406.3:n.140+31198G>A |