Canonical Allele Identifier:
CA1475304992
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89655779C= , CM000666.2:g.89655779C= | GRCh38 |
| NC_000004.11:g.90576930C= , CM000666.1:g.90576930C= | GRCh37 |
| NC_000004.10:g.90795953C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938986.1:n.434+27862C= | ||
| XR_938987.1:n.688+27862C= | ||
| XR_938988.1:n.554+27862C= | ||
| XR_938990.1:n.299-35506C= | ||
| XR_938991.1:n.434+27862C= | ||
| XR_938994.1:n.779+27862C= | ||
| XR_938995.1:n.613+27862C= | ||
| XR_938986.2:n.459+27862C= | ||
| XR_938987.2:n.748+27862C= |