Canonical Allele Identifier: CA2298481316
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477846C= , CM000680.2:g.41477846C= GRCh38
NC_000018.9:g.39057810C= , CM000680.1:g.39057810C= GRCh37
NC_000018.8:g.37311808C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935409.1:n.86-26288C=