Canonical Allele Identifier:
CA799753477
Gene:
Linked Data
dbSNP Id:
rs1277975623
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89655729C>T , CM000666.2:g.89655729C>T | GRCh38 |
| NC_000004.11:g.90576880C>T , CM000666.1:g.90576880C>T | GRCh37 |
| NC_000004.10:g.90795903C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938986.1:n.434+27812C>T | ||
| XR_938987.1:n.688+27812C>T | ||
| XR_938988.1:n.554+27812C>T | ||
| XR_938990.1:n.299-35556C>T | ||
| XR_938991.1:n.434+27812C>T | ||
| XR_938994.1:n.779+27812C>T | ||
| XR_938995.1:n.613+27812C>T | ||
| XR_938986.2:n.459+27812C>T | ||
| XR_938987.2:n.748+27812C>T |