Canonical Allele Identifier:
CA1439212625
Gene:
Linked Data
dbSNP Id:
rs1577128430
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12578012T>A , CM000666.2:g.12578012T>A | GRCh38 |
| NC_000004.11:g.12579636T>A , CM000666.1:g.12579636T>A | GRCh37 |
| NC_000004.10:g.12188734T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_925406.1:n.106+31330A>T | ||
| XR_001741374.1:n.254+44643A>T | ||
| XR_925406.3:n.140+31330A>T |