Canonical Allele Identifier:
CA1475304969
Gene:
Linked Data
dbSNP Id:
rs1722646659
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89655732G>T , CM000666.2:g.89655732G>T | GRCh38 |
| NC_000004.11:g.90576883G>T , CM000666.1:g.90576883G>T | GRCh37 |
| NC_000004.10:g.90795906G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938986.1:n.434+27815G>T | ||
| XR_938987.1:n.688+27815G>T | ||
| XR_938988.1:n.554+27815G>T | ||
| XR_938990.1:n.299-35553G>T | ||
| XR_938991.1:n.434+27815G>T | ||
| XR_938994.1:n.779+27815G>T | ||
| XR_938995.1:n.613+27815G>T | ||
| XR_938986.2:n.459+27815G>T | ||
| XR_938987.2:n.748+27815G>T |